ENST00000624552.4:c.14942T>G
|
ENSP00000485357.2:p.Val4981Gly
|
|
ENST00000683500.2:c.14999T>G
MANE Select
|
ENSP00000508292.2:p.Val5000Gly
|
|
ENST00000623487.1:n.3345T>G
|
|
|
ENST00000624552.3:c.14939T>G
|
ENSP00000485357.1:p.Val4980Gly
|
|
NM_001291815.1:c.14999T>G
|
NP_001278744.1:p.Val5000Gly
|
|
XM_011518465.1:c.14876T>G
|
XP_011516767.1:p.Val4959Gly
|
|
XM_011518466.1:c.14867T>G
|
XP_011516768.1:p.Val4956Gly
|
|
XM_011518467.1:c.14822T>G
|
XP_011516769.1:p.Val4941Gly
|
|
NM_001291815.2:c.14999T>G
MANE Select
|
NP_001278744.1:p.Val5000Gly
|
|
XM_011518465.2:c.14876T>G
|
XP_011516767.1:p.Val4959Gly
|
|
XM_011518466.2:c.14867T>G
|
XP_011516768.1:p.Val4956Gly
|
|
XM_011518467.2:c.14822T>G
|
XP_011516769.1:p.Val4941Gly
|
|
XM_017014585.1:c.11780T>G
|
XP_016870074.1:p.Val3927Gly
|
|
XM_017014586.1:c.7577T>G
|
XP_016870075.1:p.Val2526Gly
|
|
XR_001746957.1:n.92+169A>C
|
|
|
XR_001746958.1:n.92+169A>C
|
|
|