ENST00000262494.13:c.599T>A
|
ENSP00000262494.7:p.Phe200Tyr
|
|
ENST00000262493.12:c.599T>A
MANE Select
|
ENSP00000262493.6:p.Phe200Tyr
|
|
ENST00000262494.12:c.599T>A
|
ENSP00000262494.7:p.Phe200Tyr
|
|
ENST00000562316.6:c.266T>A
|
ENSP00000457238.2:p.Phe89Tyr
|
|
ENST00000638185.1:n.814T>A
|
|
|
ENST00000638210.1:n.899T>A
|
|
|
ENST00000638705.1:c.599T>A
|
ENSP00000491223.1:p.Phe200Tyr
|
|
ENST00000638836.1:n.509T>A
|
|
|
ENST00000639055.1:n.1320T>A
|
|
|
ENST00000639251.1:n.500T>A
|
|
|
ENST00000639268.1:c.234T>A
|
|
|
ENST00000639341.1:c.124T>A
|
|
|
ENST00000639770.1:c.637T>A
|
ENSP00000491999.1:n.637T>A
|
|
ENST00000640390.1:n.529T>A
|
|
|
ENST00000640560.1:n.375T>A
|
|
|
ENST00000640893.1:c.438T>A
|
ENSP00000492677.1:p.Val146=
|
|
ENST00000262493.10:c.599T>A
|
ENSP00000262493.6:p.Phe200Tyr
|
|
ENST00000262494.11:c.599T>A
|
ENSP00000262494.7:p.Phe200Tyr
|
|
NM_020988.2:c.599T>A
|
NP_066268.1:p.Phe200Tyr
|
|
NM_138736.2:c.599T>A
|
NP_620073.2:p.Phe200Tyr
|
|
XM_011523003.1:c.473T>A
|
XP_011521305.1:p.Phe158Tyr
|
|
XM_011523003.3:c.473T>A
|
XP_011521305.1:p.Phe158Tyr
|
|
NM_020988.3:c.599T>A
MANE Select
|
NP_066268.1:p.Phe200Tyr
|
|
NM_138736.3:c.599T>A
|
NP_620073.2:p.Phe200Tyr
|
|