ENST00000237596.7:c.1506T>A
MANE Select
|
ENSP00000237596.2:p.Tyr502Ter
|
|
ENST00000237596.6:c.1506T>A
|
ENSP00000237596.2:p.Tyr502Ter
|
|
ENST00000508588.5:c.-199+3371T>A
|
ENSP00000427131.1:n.-199+3371T>A
|
|
NM_000297.3:c.1506T>A
|
NP_000288.1:p.Tyr502Ter
|
|
XM_011532028.1:c.1281T>A
|
XP_011530330.1:p.Tyr427Ter
|
|
XM_011532029.1:c.786T>A
|
XP_011530331.1:p.Tyr262Ter
|
|
XM_011532030.1:c.666T>A
|
XP_011530332.1:p.Tyr222Ter
|
|
XR_244632.2:n.1601T>A
|
|
|
NR_156488.1:n.1593T>A
|
|
|
XM_011532028.2:c.1281T>A
|
XP_011530330.1:p.Tyr427Ter
|
|
XM_011532030.2:c.666T>A
|
XP_011530332.1:p.Tyr222Ter
|
|
NM_000297.4:c.1506T>A
MANE Select
|
NP_000288.1:p.Tyr502Ter
|
|
NR_156488.2:n.1605T>A
|
|
|