ENST00000318158.11:c.799G>C
MANE Select
|
ENSP00000313432.6:p.Gly267Arg
|
|
ENST00000318158.10:c.799G>C
|
ENSP00000313432.6:p.Gly267Arg
|
|
ENST00000460882.5:n.826G>C
|
|
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ENST00000480596.5:n.1500G>C
|
|
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ENST00000482603.1:n.252G>C
|
|
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ENST00000491488.5:n.504G>C
|
|
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ENST00000494290.1:c.*51+921G>C
|
ENSP00000432021.1:n.*51+921G>C
|
|
ENST00000497693.1:n.4367G>C
|
|
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ENST00000607784.1:c.799G>C
|
ENSP00000475569.1:p.Gly267Arg
|
|
NM_012203.1:c.799G>C
|
NP_036335.1:p.Gly267Arg
|
|
XM_005251631.1:c.478G>C
|
XP_005251688.1:p.Gly160Arg
|
|
XM_011518073.1:c.397G>C
|
XP_011516375.1:p.Gly133Arg
|
|
XM_017015320.2:c.799G>C
|
XP_016870809.1:p.Gly267Arg
|
|
XM_017015321.2:c.799G>C
|
XP_016870810.1:p.Gly267Arg
|
|
XM_017015323.2:c.397G>C
|
XP_016870812.1:p.Gly133Arg
|
|
XM_024447716.1:c.1072G>C
|
XP_024303484.1:p.Gly358Arg
|
|
XM_024447717.1:c.1072G>C
|
XP_024303485.1:p.Gly358Arg
|
|
XR_002956828.1:n.1087G>C
|
|
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XR_002956829.1:n.1087G>C
|
|
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XR_002956830.1:n.2219G>C
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|
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XR_002956831.1:n.1894G>C
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|
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XR_002956832.1:n.1218G>C
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|
|
NM_012203.2:c.799G>C
MANE Select
|
NP_036335.1:p.Gly267Arg
|
|