ENST00000216373.10:c.398T>G
MANE Select
|
ENSP00000216373.5:p.Val133Gly
|
|
ENST00000216373.9:c.398T>G
|
ENSP00000216373.5:p.Val133Gly
|
|
ENST00000543680.5:c.398T>G
|
ENSP00000445328.1:p.Val133Gly
|
|
ENST00000555666.1:n.577T>G
|
|
|
ENST00000556469.5:n.369T>G
|
|
|
NM_006939.2:c.398T>G
|
NP_008870.2:p.Val133Gly
|
|
XM_005268021.1:c.218T>G
|
XP_005268078.1:p.Val73Gly
|
|
XM_011537103.1:c.359T>G
|
XP_011535405.1:p.Val120Gly
|
|
XM_011537104.1:c.398T>G
|
XP_011535406.1:p.Val133Gly
|
|
XR_943842.1:n.1039+15931A>C
|
|
|
XR_943843.1:n.1039+15931A>C
|
|
|
NM_006939.3:c.398T>G
|
NP_008870.2:p.Val133Gly
|
|
NM_006939.4:c.398T>G
MANE Select
|
NP_008870.2:p.Val133Gly
|
|