ENST00000273283.7:c.1800T>C
MANE Select
|
ENSP00000273283.2:p.Tyr600=
|
|
ENST00000273283.6:c.1800T>C
|
ENSP00000273283.2:p.Tyr600=
|
|
ENST00000428133.5:c.459T>C
|
ENSP00000395836.1:p.Tyr153=
|
|
ENST00000484844.2:c.67T>C
|
|
|
ENST00000537050.5:c.936T>C
|
ENSP00000443847.1:p.Tyr312=
|
|
ENST00000628722.2:n.1655T>C
|
|
|
NM_001166434.2:c.1374T>C
|
NP_001159906.1:p.Tyr458=
|
|
NM_001166435.2:c.936T>C
|
NP_001159907.1:p.Tyr312=
|
|
NM_001166436.2:c.936T>C
|
NP_001159908.1:p.Tyr312=
|
|
NM_002215.3:c.1800T>C
|
NP_002206.2:p.Tyr600=
|
|
NM_002215.4:c.1800T>C
MANE Select
|
NP_002206.2:p.Tyr600=
|
|
NM_001166434.3:c.1374T>C
|
NP_001159906.1:p.Tyr458=
|
|