ENST00000624552.4:c.14939A>C
|
ENSP00000485357.2:p.Asp4980Ala
|
|
ENST00000683500.2:c.14996A>C
MANE Select
|
ENSP00000508292.2:p.Asp4999Ala
|
|
ENST00000623487.1:n.3342A>C
|
|
|
ENST00000624552.3:c.14936A>C
|
ENSP00000485357.1:p.Asp4979Ala
|
|
NM_001291815.1:c.14996A>C
|
NP_001278744.1:p.Asp4999Ala
|
|
XM_011518465.1:c.14873A>C
|
XP_011516767.1:p.Asp4958Ala
|
|
XM_011518466.1:c.14864A>C
|
XP_011516768.1:p.Asp4955Ala
|
|
XM_011518467.1:c.14819A>C
|
XP_011516769.1:p.Asp4940Ala
|
|
NM_001291815.2:c.14996A>C
MANE Select
|
NP_001278744.1:p.Asp4999Ala
|
|
XM_011518465.2:c.14873A>C
|
XP_011516767.1:p.Asp4958Ala
|
|
XM_011518466.2:c.14864A>C
|
XP_011516768.1:p.Asp4955Ala
|
|
XM_011518467.2:c.14819A>C
|
XP_011516769.1:p.Asp4940Ala
|
|
XM_017014585.1:c.11777A>C
|
XP_016870074.1:p.Asp3926Ala
|
|
XM_017014586.1:c.7574A>C
|
XP_016870075.1:p.Asp2525Ala
|
|
XR_001746957.1:n.92+172T>G
|
|
|
XR_001746958.1:n.92+172T>G
|
|
|