ENST00000624552.4:c.14920G>T
|
ENSP00000485357.2:p.Gly4974Cys
|
|
ENST00000683500.2:c.14977G>T
MANE Select
|
ENSP00000508292.2:p.Gly4993Cys
|
|
ENST00000623487.1:n.3323G>T
|
|
|
ENST00000624552.3:c.14917G>T
|
ENSP00000485357.1:p.Gly4973Cys
|
|
NM_001291815.1:c.14977G>T
|
NP_001278744.1:p.Gly4993Cys
|
|
XM_011518465.1:c.14854G>T
|
XP_011516767.1:p.Gly4952Cys
|
|
XM_011518466.1:c.14845G>T
|
XP_011516768.1:p.Gly4949Cys
|
|
XM_011518467.1:c.14800G>T
|
XP_011516769.1:p.Gly4934Cys
|
|
NM_001291815.2:c.14977G>T
MANE Select
|
NP_001278744.1:p.Gly4993Cys
|
|
XM_011518465.2:c.14854G>T
|
XP_011516767.1:p.Gly4952Cys
|
|
XM_011518466.2:c.14845G>T
|
XP_011516768.1:p.Gly4949Cys
|
|
XM_011518467.2:c.14800G>T
|
XP_011516769.1:p.Gly4934Cys
|
|
XM_017014585.1:c.11758G>T
|
XP_016870074.1:p.Gly3920Cys
|
|
XM_017014586.1:c.7555G>T
|
XP_016870075.1:p.Gly2519Cys
|
|
XR_001746957.1:n.92+191C>A
|
|
|
XR_001746958.1:n.92+191C>A
|
|
|