ENST00000650793.2:n.542A>T
|
|
|
ENST00000697612.1:n.1220A>T
|
|
|
ENST00000374881.3:c.351A>T
|
ENSP00000364015.2:p.Ala117=
|
|
ENST00000374882.8:c.363A>T
MANE Select
|
ENSP00000364016.4:p.Ala121=
|
|
ENST00000650411.1:n.1684A>T
|
|
|
ENST00000650793.1:n.542A>T
|
|
|
ENST00000374881.2:c.351A>T
|
ENSP00000364015.2:p.Ala117=
|
|
ENST00000374882.7:c.363A>T
|
ENSP00000364016.3:p.Ala121=
|
|
ENST00000395339.7:c.296-5A>T
|
ENSP00000378748.3:n.296-5A>T
|
|
ENST00000484003.1:n.747A>T
|
|
|
NM_004159.4:c.351A>T
|
NP_004150.1:p.Ala117=
|
|
NM_148919.3:c.363A>T
|
NP_683720.2:p.Ala121=
|
|
NM_148919.4:c.363A>T
MANE Select
|
NP_683720.2:p.Ala121=
|
|
NM_004159.5:c.351A>T
|
NP_004150.1:p.Ala117=
|
|