ENST00000624552.4:c.14930C>A
|
ENSP00000485357.2:p.Ala4977Asp
|
|
ENST00000683500.2:c.14987C>A
MANE Select
|
ENSP00000508292.2:p.Ala4996Asp
|
|
ENST00000623487.1:n.3333C>A
|
|
|
ENST00000624552.3:c.14927C>A
|
ENSP00000485357.1:p.Ala4976Asp
|
|
NM_001291815.1:c.14987C>A
|
NP_001278744.1:p.Ala4996Asp
|
|
XM_011518465.1:c.14864C>A
|
XP_011516767.1:p.Ala4955Asp
|
|
XM_011518466.1:c.14855C>A
|
XP_011516768.1:p.Ala4952Asp
|
|
XM_011518467.1:c.14810C>A
|
XP_011516769.1:p.Ala4937Asp
|
|
NM_001291815.2:c.14987C>A
MANE Select
|
NP_001278744.1:p.Ala4996Asp
|
|
XM_011518465.2:c.14864C>A
|
XP_011516767.1:p.Ala4955Asp
|
|
XM_011518466.2:c.14855C>A
|
XP_011516768.1:p.Ala4952Asp
|
|
XM_011518467.2:c.14810C>A
|
XP_011516769.1:p.Ala4937Asp
|
|
XM_017014585.1:c.11768C>A
|
XP_016870074.1:p.Ala3923Asp
|
|
XM_017014586.1:c.7565C>A
|
XP_016870075.1:p.Ala2522Asp
|
|
XR_001746957.1:n.92+181G>T
|
|
|
XR_001746958.1:n.92+181G>T
|
|
|