ENST00000216373.10:c.444T>C
MANE Select
|
ENSP00000216373.5:p.Tyr148=
|
|
ENST00000216373.9:c.444T>C
|
ENSP00000216373.5:p.Tyr148=
|
|
ENST00000543680.5:c.444T>C
|
ENSP00000445328.1:p.Tyr148=
|
|
ENST00000555666.1:n.623T>C
|
|
|
ENST00000556469.5:n.415T>C
|
|
|
NM_006939.2:c.444T>C
|
NP_008870.2:p.Tyr148=
|
|
XM_005268021.1:c.264T>C
|
XP_005268078.1:p.Tyr88=
|
|
XM_011537103.1:c.405T>C
|
XP_011535405.1:p.Tyr135=
|
|
XM_011537104.1:c.444T>C
|
XP_011535406.1:p.Tyr148=
|
|
XR_943842.1:n.1039+15885A>G
|
|
|
XR_943843.1:n.1039+15885A>G
|
|
|
NM_006939.3:c.444T>C
|
NP_008870.2:p.Tyr148=
|
|
NM_006939.4:c.444T>C
MANE Select
|
NP_008870.2:p.Tyr148=
|
|