ENST00000624552.4:c.14945C>A
|
ENSP00000485357.2:p.Ala4982Asp
|
|
ENST00000683500.2:c.15002C>A
MANE Select
|
ENSP00000508292.2:p.Ala5001Asp
|
|
ENST00000623487.1:n.3348C>A
|
|
|
ENST00000624552.3:c.14942C>A
|
ENSP00000485357.1:p.Ala4981Asp
|
|
NM_001291815.1:c.15002C>A
|
NP_001278744.1:p.Ala5001Asp
|
|
XM_011518465.1:c.14879C>A
|
XP_011516767.1:p.Ala4960Asp
|
|
XM_011518466.1:c.14870C>A
|
XP_011516768.1:p.Ala4957Asp
|
|
XM_011518467.1:c.14825C>A
|
XP_011516769.1:p.Ala4942Asp
|
|
NM_001291815.2:c.15002C>A
MANE Select
|
NP_001278744.1:p.Ala5001Asp
|
|
XM_011518465.2:c.14879C>A
|
XP_011516767.1:p.Ala4960Asp
|
|
XM_011518466.2:c.14870C>A
|
XP_011516768.1:p.Ala4957Asp
|
|
XM_011518467.2:c.14825C>A
|
XP_011516769.1:p.Ala4942Asp
|
|
XM_017014585.1:c.11783C>A
|
XP_016870074.1:p.Ala3928Asp
|
|
XM_017014586.1:c.7580C>A
|
XP_016870075.1:p.Ala2527Asp
|
|
XR_001746957.1:n.92+166G>T
|
|
|
XR_001746958.1:n.92+166G>T
|
|
|