ENST00000225927.7:c.1913A>G
MANE Select
|
ENSP00000225927.1:p.Tyr638Cys
|
|
ENST00000225927.6:c.1913A>G
|
ENSP00000225927.1:p.Tyr638Cys
|
|
ENST00000591587.1:c.1251A>G
|
ENSP00000467836.1:n.1251A>G
|
|
NM_000263.3:c.1913A>G
|
NP_000254.2:p.Tyr638Cys
|
|
XM_006721920.2:c.1082A>G
|
XP_006721983.1:p.Tyr361Cys
|
|
XM_011524840.1:c.914A>G
|
XP_011523142.1:p.Tyr305Cys
|
|
XM_017024687.1:c.1082A>G
|
XP_016880176.1:p.Tyr361Cys
|
|
XM_024450771.1:c.1970A>G
|
XP_024306539.1:p.Tyr657Cys
|
|
XM_024450772.1:c.914A>G
|
XP_024306540.1:p.Tyr305Cys
|
|
NM_000263.4:c.1913A>G
MANE Select
|
NP_000254.2:p.Tyr638Cys
|
|