ENST00000624552.4:c.14940C>G
|
ENSP00000485357.2:p.Asp4980Glu
|
|
ENST00000683500.2:c.14997C>G
MANE Select
|
ENSP00000508292.2:p.Asp4999Glu
|
|
ENST00000623487.1:n.3343C>G
|
|
|
ENST00000624552.3:c.14937C>G
|
ENSP00000485357.1:p.Asp4979Glu
|
|
NM_001291815.1:c.14997C>G
|
NP_001278744.1:p.Asp4999Glu
|
|
XM_011518465.1:c.14874C>G
|
XP_011516767.1:p.Asp4958Glu
|
|
XM_011518466.1:c.14865C>G
|
XP_011516768.1:p.Asp4955Glu
|
|
XM_011518467.1:c.14820C>G
|
XP_011516769.1:p.Asp4940Glu
|
|
NM_001291815.2:c.14997C>G
MANE Select
|
NP_001278744.1:p.Asp4999Glu
|
|
XM_011518465.2:c.14874C>G
|
XP_011516767.1:p.Asp4958Glu
|
|
XM_011518466.2:c.14865C>G
|
XP_011516768.1:p.Asp4955Glu
|
|
XM_011518467.2:c.14820C>G
|
XP_011516769.1:p.Asp4940Glu
|
|
XM_017014585.1:c.11778C>G
|
XP_016870074.1:p.Asp3926Glu
|
|
XM_017014586.1:c.7575C>G
|
XP_016870075.1:p.Asp2525Glu
|
|
XR_001746957.1:n.92+171G>C
|
|
|
XR_001746958.1:n.92+171G>C
|
|
|