ENST00000624552.4:c.14957C>T
|
ENSP00000485357.2:p.Ala4986Val
|
|
ENST00000683500.2:c.15014C>T
MANE Select
|
ENSP00000508292.2:p.Ala5005Val
|
|
ENST00000623487.1:n.3360C>T
|
|
|
ENST00000624552.3:c.14954C>T
|
ENSP00000485357.1:p.Ala4985Val
|
|
NM_001291815.1:c.15014C>T
|
NP_001278744.1:p.Ala5005Val
|
|
XM_011518465.1:c.14891C>T
|
XP_011516767.1:p.Ala4964Val
|
|
XM_011518466.1:c.14882C>T
|
XP_011516768.1:p.Ala4961Val
|
|
XM_011518467.1:c.14837C>T
|
XP_011516769.1:p.Ala4946Val
|
|
NM_001291815.2:c.15014C>T
MANE Select
|
NP_001278744.1:p.Ala5005Val
|
|
XM_011518465.2:c.14891C>T
|
XP_011516767.1:p.Ala4964Val
|
|
XM_011518466.2:c.14882C>T
|
XP_011516768.1:p.Ala4961Val
|
|
XM_011518467.2:c.14837C>T
|
XP_011516769.1:p.Ala4946Val
|
|
XM_017014585.1:c.11795C>T
|
XP_016870074.1:p.Ala3932Val
|
|
XM_017014586.1:c.7592C>T
|
XP_016870075.1:p.Ala2531Val
|
|
XR_001746957.1:n.92+154G>A
|
|
|
XR_001746958.1:n.92+154G>A
|
|
|