ENST00000348127.11:c.911A>C
|
ENSP00000265385.8:p.Asp304Ala
|
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ENST00000484496.6:n.894A>C
|
|
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ENST00000338791.11:c.1019A>C
MANE Select
|
ENSP00000345096.6:p.Asp340Ala
|
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ENST00000648462.1:c.651A>C
|
|
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ENST00000338791.10:c.1019A>C
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ENSP00000345096.6:p.Asp340Ala
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|
ENST00000348127.10:c.911A>C
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ENSP00000265385.8:p.Asp304Ala
|
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ENST00000354269.9:c.989A>C
|
ENSP00000346219.5:p.Asp330Ala
|
|
ENST00000419067.6:c.920A>C
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ENSP00000399400.2:p.Asp307Ala
|
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ENST00000469328.5:c.784A>C
|
|
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ENST00000470772.5:c.761A>C
|
ENSP00000417296.1:p.Asp254Ala
|
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ENST00000480861.5:c.749A>C
|
ENSP00000420185.1:p.Asp250Ala
|
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ENST00000484496.5:c.894A>C
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ENSP00000418742.1:n.894A>C
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ENST00000496200.5:c.689A>C
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ENSP00000420803.1:p.Asp230Ala
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|
ENST00000497868.5:c.812A>C
|
ENSP00000419609.1:p.Asp271Ala
|
|
ENST00000626419.2:c.761A>C
|
ENSP00000486056.1:p.Asp254Ala
|
|
NM_000883.3:c.1019A>C
|
NP_000874.2:p.Asp340Ala
|
|
NM_001102605.1:c.989A>C
|
NP_001096075.1:p.Asp330Ala
|
|
NM_001142573.1:c.764A>C
|
NP_001136045.1:p.Asp255Ala
|
|
NM_001142574.1:c.749A>C
|
NP_001136046.1:p.Asp250Ala
|
|
NM_001142575.1:c.689A>C
|
NP_001136047.1:p.Asp230Ala
|
|
NM_001142576.1:c.920A>C
|
NP_001136048.1:p.Asp307Ala
|
|
NM_001304521.1:c.812A>C
|
NP_001291450.1:p.Asp271Ala
|
|
NM_183243.2:c.911A>C
|
NP_899066.1:p.Asp304Ala
|
|
XM_005250314.1:c.788A>C
|
XP_005250371.1:p.Asp263Ala
|
|
XM_006715967.1:c.1019A>C
|
XP_006716030.1:p.Asp340Ala
|
|
XM_006715968.1:c.989A>C
|
XP_006716031.1:p.Asp330Ala
|
|
XM_006715969.1:c.911A>C
|
XP_006716032.1:p.Asp304Ala
|
|
XM_006715970.2:c.812A>C
|
XP_006716033.1:p.Asp271Ala
|
|
XM_006715971.1:c.788A>C
|
XP_006716034.1:p.Asp263Ala
|
|
XM_011516156.1:c.401A>C
|
XP_011514458.1:p.Asp134Ala
|
|
XM_011516157.1:c.401A>C
|
XP_011514459.1:p.Asp134Ala
|
|
XM_017012172.1:c.788A>C
|
XP_016867661.1:p.Asp263Ala
|
|
XM_017012173.1:c.989A>C
|
XP_016867662.1:p.Asp330Ala
|
|
XM_024446755.1:c.989A>C
|
XP_024302523.1:p.Asp330Ala
|
|
XM_024446756.1:c.911A>C
|
XP_024302524.1:p.Asp304Ala
|
|
XM_024446757.1:c.812A>C
|
XP_024302525.1:p.Asp271Ala
|
|
XM_024446758.1:c.788A>C
|
XP_024302526.1:p.Asp263Ala
|
|
NM_000883.4:c.1019A>C
MANE Select
|
NP_000874.2:p.Asp340Ala
|
|
NM_001102605.2:c.989A>C
|
NP_001096075.1:p.Asp330Ala
|
|
NM_001142573.2:c.764A>C
|
NP_001136045.1:p.Asp255Ala
|
|
NM_001142574.2:c.749A>C
|
NP_001136046.1:p.Asp250Ala
|
|
NM_001142575.2:c.689A>C
|
NP_001136047.1:p.Asp230Ala
|
|
NM_001142576.2:c.920A>C
|
NP_001136048.1:p.Asp307Ala
|
|
NM_001304521.2:c.812A>C
|
NP_001291450.1:p.Asp271Ala
|
|
NM_183243.3:c.911A>C
|
NP_899066.1:p.Asp304Ala
|
|