ENST00000624552.4:c.14938G>T
|
ENSP00000485357.2:p.Asp4980Tyr
|
|
ENST00000683500.2:c.14995G>T
MANE Select
|
ENSP00000508292.2:p.Asp4999Tyr
|
|
ENST00000623487.1:n.3341G>T
|
|
|
ENST00000624552.3:c.14935G>T
|
ENSP00000485357.1:p.Asp4979Tyr
|
|
NM_001291815.1:c.14995G>T
|
NP_001278744.1:p.Asp4999Tyr
|
|
XM_011518465.1:c.14872G>T
|
XP_011516767.1:p.Asp4958Tyr
|
|
XM_011518466.1:c.14863G>T
|
XP_011516768.1:p.Asp4955Tyr
|
|
XM_011518467.1:c.14818G>T
|
XP_011516769.1:p.Asp4940Tyr
|
|
NM_001291815.2:c.14995G>T
MANE Select
|
NP_001278744.1:p.Asp4999Tyr
|
|
XM_011518465.2:c.14872G>T
|
XP_011516767.1:p.Asp4958Tyr
|
|
XM_011518466.2:c.14863G>T
|
XP_011516768.1:p.Asp4955Tyr
|
|
XM_011518467.2:c.14818G>T
|
XP_011516769.1:p.Asp4940Tyr
|
|
XM_017014585.1:c.11776G>T
|
XP_016870074.1:p.Asp3926Tyr
|
|
XM_017014586.1:c.7573G>T
|
XP_016870075.1:p.Asp2525Tyr
|
|
XR_001746957.1:n.92+173C>A
|
|
|
XR_001746958.1:n.92+173C>A
|
|
|