ENST00000624552.4:c.14920G>C
|
ENSP00000485357.2:p.Gly4974Arg
|
|
ENST00000683500.2:c.14977G>C
MANE Select
|
ENSP00000508292.2:p.Gly4993Arg
|
|
ENST00000623487.1:n.3323G>C
|
|
|
ENST00000624552.3:c.14917G>C
|
ENSP00000485357.1:p.Gly4973Arg
|
|
NM_001291815.1:c.14977G>C
|
NP_001278744.1:p.Gly4993Arg
|
|
XM_011518465.1:c.14854G>C
|
XP_011516767.1:p.Gly4952Arg
|
|
XM_011518466.1:c.14845G>C
|
XP_011516768.1:p.Gly4949Arg
|
|
XM_011518467.1:c.14800G>C
|
XP_011516769.1:p.Gly4934Arg
|
|
NM_001291815.2:c.14977G>C
MANE Select
|
NP_001278744.1:p.Gly4993Arg
|
|
XM_011518465.2:c.14854G>C
|
XP_011516767.1:p.Gly4952Arg
|
|
XM_011518466.2:c.14845G>C
|
XP_011516768.1:p.Gly4949Arg
|
|
XM_011518467.2:c.14800G>C
|
XP_011516769.1:p.Gly4934Arg
|
|
XM_017014585.1:c.11758G>C
|
XP_016870074.1:p.Gly3920Arg
|
|
XM_017014586.1:c.7555G>C
|
XP_016870075.1:p.Gly2519Arg
|
|
XR_001746957.1:n.92+191C>G
|
|
|
XR_001746958.1:n.92+191C>G
|
|
|