ENST00000703783.1:n.569G>T
|
|
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ENST00000703785.1:n.650G>T
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|
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ENST00000262464.9:c.3785G>T
MANE Select
|
ENSP00000262464.4:p.Gly1262Val
|
|
ENST00000262464.8:c.3785G>T
|
ENSP00000262464.4:p.Gly1262Val
|
|
ENST00000507835.5:c.335G>T
|
ENSP00000426839.1:p.Gly112Val
|
|
ENST00000508053.5:c.3785G>T
|
ENSP00000424571.1:p.Gly1262Val
|
|
ENST00000508989.5:c.3686G>T
|
ENSP00000425596.1:p.Gly1229Val
|
|
ENST00000619499.4:c.3782G>T
|
ENSP00000482132.1:p.Gly1261Val
|
|
NM_001999.3:c.3785G>T
|
NP_001990.2:p.Gly1262Val
|
|
XM_017009228.2:c.3632G>T
|
XP_016864717.1:p.Gly1211Val
|
|
NM_001999.4:c.3785G>T
MANE Select
|
NP_001990.2:p.Gly1262Val
|
|