ENST00000559133.6:c.5696C=
|
ENSP00000453958.2:p.Ala1899=
|
|
ENST00000674301.2:c.5696C=
|
ENSP00000501333.2:p.Ala1899=
|
|
ENST00000684448.1:n.4370C=
|
|
|
ENST00000316623.10:c.5696C=
MANE Select
|
ENSP00000325527.5:p.Ala1899=
|
|
ENST00000674301.1:c.695C=
|
ENSP00000501333.1:p.Ala232=
|
|
ENST00000316623.9:c.5696C=
|
ENSP00000325527.5:p.Ala1899=
|
|
ENST00000537463.6:c.*1459C=
|
ENSP00000440294.2:n.*1459C=
|
|
ENST00000559133.5:c.1003C=
|
|
|
NM_000138.4:c.5696C= , LRG_778t1:c.5696C=
|
NP_000129.3:p.Ala1899=
|
|
NM_000138.5:c.5696C=
MANE Select
|
NP_000129.3:p.Ala1899=
|
|