ENST00000624552.4:c.14930C>G
|
ENSP00000485357.2:p.Ala4977Gly
|
|
ENST00000683500.2:c.14987C>G
MANE Select
|
ENSP00000508292.2:p.Ala4996Gly
|
|
ENST00000623487.1:n.3333C>G
|
|
|
ENST00000624552.3:c.14927C>G
|
ENSP00000485357.1:p.Ala4976Gly
|
|
NM_001291815.1:c.14987C>G
|
NP_001278744.1:p.Ala4996Gly
|
|
XM_011518465.1:c.14864C>G
|
XP_011516767.1:p.Ala4955Gly
|
|
XM_011518466.1:c.14855C>G
|
XP_011516768.1:p.Ala4952Gly
|
|
XM_011518467.1:c.14810C>G
|
XP_011516769.1:p.Ala4937Gly
|
|
NM_001291815.2:c.14987C>G
MANE Select
|
NP_001278744.1:p.Ala4996Gly
|
|
XM_011518465.2:c.14864C>G
|
XP_011516767.1:p.Ala4955Gly
|
|
XM_011518466.2:c.14855C>G
|
XP_011516768.1:p.Ala4952Gly
|
|
XM_011518467.2:c.14810C>G
|
XP_011516769.1:p.Ala4937Gly
|
|
XM_017014585.1:c.11768C>G
|
XP_016870074.1:p.Ala3923Gly
|
|
XM_017014586.1:c.7565C>G
|
XP_016870075.1:p.Ala2522Gly
|
|
XR_001746957.1:n.92+181G>C
|
|
|
XR_001746958.1:n.92+181G>C
|
|
|