ENST00000624552.4:c.14929G>A
|
ENSP00000485357.2:p.Ala4977Thr
|
|
ENST00000683500.2:c.14986G>A
MANE Select
|
ENSP00000508292.2:p.Ala4996Thr
|
|
ENST00000623487.1:n.3332G>A
|
|
|
ENST00000624552.3:c.14926G>A
|
ENSP00000485357.1:p.Ala4976Thr
|
|
NM_001291815.1:c.14986G>A
|
NP_001278744.1:p.Ala4996Thr
|
|
XM_011518465.1:c.14863G>A
|
XP_011516767.1:p.Ala4955Thr
|
|
XM_011518466.1:c.14854G>A
|
XP_011516768.1:p.Ala4952Thr
|
|
XM_011518467.1:c.14809G>A
|
XP_011516769.1:p.Ala4937Thr
|
|
NM_001291815.2:c.14986G>A
MANE Select
|
NP_001278744.1:p.Ala4996Thr
|
|
XM_011518465.2:c.14863G>A
|
XP_011516767.1:p.Ala4955Thr
|
|
XM_011518466.2:c.14854G>A
|
XP_011516768.1:p.Ala4952Thr
|
|
XM_011518467.2:c.14809G>A
|
XP_011516769.1:p.Ala4937Thr
|
|
XM_017014585.1:c.11767G>A
|
XP_016870074.1:p.Ala3923Thr
|
|
XM_017014586.1:c.7564G>A
|
XP_016870075.1:p.Ala2522Thr
|
|
XR_001746957.1:n.92+182C>T
|
|
|
XR_001746958.1:n.92+182C>T
|
|
|