ENST00000624552.4:c.14922C>T
|
ENSP00000485357.2:p.Gly4974=
|
|
ENST00000683500.2:c.14979C>T
MANE Select
|
ENSP00000508292.2:p.Gly4993=
|
|
ENST00000623487.1:n.3325C>T
|
|
|
ENST00000624552.3:c.14919C>T
|
ENSP00000485357.1:p.Gly4973=
|
|
NM_001291815.1:c.14979C>T
|
NP_001278744.1:p.Gly4993=
|
|
XM_011518465.1:c.14856C>T
|
XP_011516767.1:p.Gly4952=
|
|
XM_011518466.1:c.14847C>T
|
XP_011516768.1:p.Gly4949=
|
|
XM_011518467.1:c.14802C>T
|
XP_011516769.1:p.Gly4934=
|
|
NM_001291815.2:c.14979C>T
MANE Select
|
NP_001278744.1:p.Gly4993=
|
|
XM_011518465.2:c.14856C>T
|
XP_011516767.1:p.Gly4952=
|
|
XM_011518466.2:c.14847C>T
|
XP_011516768.1:p.Gly4949=
|
|
XM_011518467.2:c.14802C>T
|
XP_011516769.1:p.Gly4934=
|
|
XM_017014585.1:c.11760C>T
|
XP_016870074.1:p.Gly3920=
|
|
XM_017014586.1:c.7557C>T
|
XP_016870075.1:p.Gly2519=
|
|
XR_001746957.1:n.92+189G>A
|
|
|
XR_001746958.1:n.92+189G>A
|
|
|