ENST00000624552.4:c.14946C>T
|
ENSP00000485357.2:p.Ala4982=
|
|
ENST00000683500.2:c.15003C>T
MANE Select
|
ENSP00000508292.2:p.Ala5001=
|
|
ENST00000623487.1:n.3349C>T
|
|
|
ENST00000624552.3:c.14943C>T
|
ENSP00000485357.1:p.Ala4981=
|
|
NM_001291815.1:c.15003C>T
|
NP_001278744.1:p.Ala5001=
|
|
XM_011518465.1:c.14880C>T
|
XP_011516767.1:p.Ala4960=
|
|
XM_011518466.1:c.14871C>T
|
XP_011516768.1:p.Ala4957=
|
|
XM_011518467.1:c.14826C>T
|
XP_011516769.1:p.Ala4942=
|
|
NM_001291815.2:c.15003C>T
MANE Select
|
NP_001278744.1:p.Ala5001=
|
|
XM_011518465.2:c.14880C>T
|
XP_011516767.1:p.Ala4960=
|
|
XM_011518466.2:c.14871C>T
|
XP_011516768.1:p.Ala4957=
|
|
XM_011518467.2:c.14826C>T
|
XP_011516769.1:p.Ala4942=
|
|
XM_017014585.1:c.11784C>T
|
XP_016870074.1:p.Ala3928=
|
|
XM_017014586.1:c.7581C>T
|
XP_016870075.1:p.Ala2527=
|
|
XR_001746957.1:n.92+165G>A
|
|
|
XR_001746958.1:n.92+165G>A
|
|
|