ENST00000348127.11:c.887G>C
|
ENSP00000265385.8:p.Gly296Ala
|
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ENST00000484496.6:n.870G>C
|
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ENST00000338791.11:c.995G>C
MANE Select
|
ENSP00000345096.6:p.Gly332Ala
|
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ENST00000648462.1:c.627G>C
|
|
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ENST00000338791.10:c.995G>C
|
ENSP00000345096.6:p.Gly332Ala
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ENST00000348127.10:c.887G>C
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ENSP00000265385.8:p.Gly296Ala
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ENST00000354269.9:c.965G>C
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ENSP00000346219.5:p.Gly322Ala
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ENST00000419067.6:c.896G>C
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ENSP00000399400.2:p.Gly299Ala
|
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ENST00000468842.1:n.584G>C
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|
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ENST00000469328.5:c.760G>C
|
|
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ENST00000470772.5:c.737G>C
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ENSP00000417296.1:p.Gly246Ala
|
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ENST00000480861.5:c.725G>C
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ENSP00000420185.1:p.Gly242Ala
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ENST00000484496.5:c.870G>C
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ENSP00000418742.1:n.870G>C
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ENST00000496200.5:c.665G>C
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ENSP00000420803.1:p.Gly222Ala
|
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ENST00000497868.5:c.788G>C
|
ENSP00000419609.1:p.Gly263Ala
|
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ENST00000626419.2:c.737G>C
|
ENSP00000486056.1:p.Gly246Ala
|
|
NM_000883.3:c.995G>C
|
NP_000874.2:p.Gly332Ala
|
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NM_001102605.1:c.965G>C
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NP_001096075.1:p.Gly322Ala
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NM_001142573.1:c.740G>C
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NP_001136045.1:p.Gly247Ala
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NM_001142574.1:c.725G>C
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NP_001136046.1:p.Gly242Ala
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NM_001142575.1:c.665G>C
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NP_001136047.1:p.Gly222Ala
|
|
NM_001142576.1:c.896G>C
|
NP_001136048.1:p.Gly299Ala
|
|
NM_001304521.1:c.788G>C
|
NP_001291450.1:p.Gly263Ala
|
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NM_183243.2:c.887G>C
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NP_899066.1:p.Gly296Ala
|
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XM_005250314.1:c.764G>C
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XP_005250371.1:p.Gly255Ala
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XM_006715967.1:c.995G>C
|
XP_006716030.1:p.Gly332Ala
|
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XM_006715968.1:c.965G>C
|
XP_006716031.1:p.Gly322Ala
|
|
XM_006715969.1:c.887G>C
|
XP_006716032.1:p.Gly296Ala
|
|
XM_006715970.2:c.788G>C
|
XP_006716033.1:p.Gly263Ala
|
|
XM_006715971.1:c.764G>C
|
XP_006716034.1:p.Gly255Ala
|
|
XM_011516156.1:c.377G>C
|
XP_011514458.1:p.Gly126Ala
|
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XM_011516157.1:c.377G>C
|
XP_011514459.1:p.Gly126Ala
|
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XM_017012172.1:c.764G>C
|
XP_016867661.1:p.Gly255Ala
|
|
XM_017012173.1:c.965G>C
|
XP_016867662.1:p.Gly322Ala
|
|
XM_024446755.1:c.965G>C
|
XP_024302523.1:p.Gly322Ala
|
|
XM_024446756.1:c.887G>C
|
XP_024302524.1:p.Gly296Ala
|
|
XM_024446757.1:c.788G>C
|
XP_024302525.1:p.Gly263Ala
|
|
XM_024446758.1:c.764G>C
|
XP_024302526.1:p.Gly255Ala
|
|
NM_000883.4:c.995G>C
MANE Select
|
NP_000874.2:p.Gly332Ala
|
|
NM_001102605.2:c.965G>C
|
NP_001096075.1:p.Gly322Ala
|
|
NM_001142573.2:c.740G>C
|
NP_001136045.1:p.Gly247Ala
|
|
NM_001142574.2:c.725G>C
|
NP_001136046.1:p.Gly242Ala
|
|
NM_001142575.2:c.665G>C
|
NP_001136047.1:p.Gly222Ala
|
|
NM_001142576.2:c.896G>C
|
NP_001136048.1:p.Gly299Ala
|
|
NM_001304521.2:c.788G>C
|
NP_001291450.1:p.Gly263Ala
|
|
NM_183243.3:c.887G>C
|
NP_899066.1:p.Gly296Ala
|
|