ENST00000624552.4:c.14944G>A
|
ENSP00000485357.2:p.Ala4982Thr
|
|
ENST00000683500.2:c.15001G>A
MANE Select
|
ENSP00000508292.2:p.Ala5001Thr
|
|
ENST00000623487.1:n.3347G>A
|
|
|
ENST00000624552.3:c.14941G>A
|
ENSP00000485357.1:p.Ala4981Thr
|
|
NM_001291815.1:c.15001G>A
|
NP_001278744.1:p.Ala5001Thr
|
|
XM_011518465.1:c.14878G>A
|
XP_011516767.1:p.Ala4960Thr
|
|
XM_011518466.1:c.14869G>A
|
XP_011516768.1:p.Ala4957Thr
|
|
XM_011518467.1:c.14824G>A
|
XP_011516769.1:p.Ala4942Thr
|
|
NM_001291815.2:c.15001G>A
MANE Select
|
NP_001278744.1:p.Ala5001Thr
|
|
XM_011518465.2:c.14878G>A
|
XP_011516767.1:p.Ala4960Thr
|
|
XM_011518466.2:c.14869G>A
|
XP_011516768.1:p.Ala4957Thr
|
|
XM_011518467.2:c.14824G>A
|
XP_011516769.1:p.Ala4942Thr
|
|
XM_017014585.1:c.11782G>A
|
XP_016870074.1:p.Ala3928Thr
|
|
XM_017014586.1:c.7579G>A
|
XP_016870075.1:p.Ala2527Thr
|
|
XR_001746957.1:n.92+167C>T
|
|
|
XR_001746958.1:n.92+167C>T
|
|
|