ENST00000624552.4:c.14942T>A
|
ENSP00000485357.2:p.Val4981Glu
|
|
ENST00000683500.2:c.14999T>A
MANE Select
|
ENSP00000508292.2:p.Val5000Glu
|
|
ENST00000623487.1:n.3345T>A
|
|
|
ENST00000624552.3:c.14939T>A
|
ENSP00000485357.1:p.Val4980Glu
|
|
NM_001291815.1:c.14999T>A
|
NP_001278744.1:p.Val5000Glu
|
|
XM_011518465.1:c.14876T>A
|
XP_011516767.1:p.Val4959Glu
|
|
XM_011518466.1:c.14867T>A
|
XP_011516768.1:p.Val4956Glu
|
|
XM_011518467.1:c.14822T>A
|
XP_011516769.1:p.Val4941Glu
|
|
NM_001291815.2:c.14999T>A
MANE Select
|
NP_001278744.1:p.Val5000Glu
|
|
XM_011518465.2:c.14876T>A
|
XP_011516767.1:p.Val4959Glu
|
|
XM_011518466.2:c.14867T>A
|
XP_011516768.1:p.Val4956Glu
|
|
XM_011518467.2:c.14822T>A
|
XP_011516769.1:p.Val4941Glu
|
|
XM_017014585.1:c.11780T>A
|
XP_016870074.1:p.Val3927Glu
|
|
XM_017014586.1:c.7577T>A
|
XP_016870075.1:p.Val2526Glu
|
|
XR_001746957.1:n.92+169A>T
|
|
|
XR_001746958.1:n.92+169A>T
|
|
|