|
NM_024593.4:c.292C>T
MANE Select
|
NP_078869.1:p.Arg98Ter
|
|
ENST00000262103.8:c.292C>T
MANE Select
|
ENSP00000262103.3:p.Arg98Ter
|
|
NM_001142857.1:c.136C>T
|
NP_001136329.1:p.Arg46Ter
|
|
NM_001142857.2:c.136C>T
|
NP_001136329.1:p.Arg46Ter
|
|
NM_001363973.1:c.136C>T
|
NP_001350902.1:p.Arg46Ter
|
|
NM_001363973.2:c.136C>T
|
NP_001350902.1:p.Arg46Ter
|
|
NM_001363973.3:c.136C>T
|
NP_001350902.1:p.Arg46Ter
|
|
NM_001363974.1:c.136C>T
|
NP_001350903.1:p.Arg46Ter
|
|
NM_001363974.2:c.136C>T
|
NP_001350903.1:p.Arg46Ter
|
|
NM_024593.3:c.292C>T
|
NP_078869.1:p.Arg98Ter
|
|
NR_024605.1:n.296C>T
|
|
|
NR_024605.2:n.253C>T
|
|
|
NR_024605.3:n.253C>T
|
|
|
NR_157026.1:n.296C>T
|
|
|
NR_157027.1:n.326-1455C>T
|
|
|
NR_157027.2:n.326-1455C>T
|
|
|
ENST00000262103.7:c.292C>T
|
ENSP00000262103.3:p.Arg98Ter
|
|
ENST00000433756.1:c.136C>T
|
ENSP00000400873.1:p.Arg46Ter
|
|
ENST00000521002.5:n.292-1455C>T
|
|
|
ENST00000521701.5:c.136C>T
|
ENSP00000430374.1:p.Arg46Ter
|
|
ENST00000521721.1:n.446C>T
|
|
|
ENST00000522254.5:c.44C>T
|
|
|
ENST00000523092.5:c.136C>T
|
ENSP00000430765.1:p.Arg46Ter
|
|
XM_005251303.1:c.292C>T
|
XP_005251360.1:p.Arg98Ter
|
|
XM_005251304.2:c.136C>T
|
XP_005251361.1:p.Arg46Ter
|
|
XM_011517589.1:c.292C>T
|
XP_011515891.1:p.Arg98Ter
|
|
XM_011517590.1:c.106C>T
|
XP_011515892.1:p.Arg36Ter
|
|
XM_011517591.1:c.106C>T
|
XP_011515893.1:p.Arg36Ter
|
|
XM_011517591.2:c.106C>T
|
XP_011515893.1:p.Arg36Ter
|
|
XM_017013827.1:c.106C>T
|
XP_016869316.1:p.Arg36Ter
|
|
XM_017013828.1:c.292C>T
|
XP_016869317.1:p.Arg98Ter
|
|
XM_024447270.1:c.292C>T
|
XP_024303038.1:p.Arg98Ter
|
|
XM_024447271.1:c.292C>T
|
XP_024303039.1:p.Arg98Ter
|
|
XM_024447272.1:c.292C>T
|
XP_024303040.1:p.Arg98Ter
|
|
XM_024447273.1:c.106C>T
|
XP_024303041.1:p.Arg36Ter
|
|
XM_024447274.1:c.106C>T
|
XP_024303042.1:p.Arg36Ter
|
|
XR_002956645.1:n.409C>T
|
|
