ENST00000682275.1:c.1192C>T
|
ENSP00000507852.1:p.Pro398Ser
|
|
ENST00000683395.1:c.1133C>T
|
|
|
ENST00000684087.1:c.1156C>T
|
ENSP00000506978.1:p.Pro386Ser
|
|
ENST00000506362.2:c.907C>T
|
ENSP00000424103.2:p.Pro303Ser
|
|
ENST00000673642.1:c.815C>T
|
ENSP00000501242.1:p.Ala272Val
|
|
ENST00000673991.1:c.1192C>T
|
ENSP00000501033.1:p.Pro398Ser
|
|
ENST00000226760.5:c.1156C>T
MANE Select
|
ENSP00000226760.1:p.Pro386Ser
|
|
ENST00000503569.5:c.1156C>T
|
ENSP00000423337.1:p.Pro386Ser
|
|
ENST00000507765.1:n.1341C>T
|
|
|
NM_001145853.1:c.1156C>T
|
NP_001139325.1:p.Pro386Ser
|
|
NM_006005.3:c.1156C>T
MANE Select
|
NP_005996.2:p.Pro386Ser
|
|
XM_017008586.1:c.1165C>T
|
XP_016864075.1:p.Pro389Ser
|
|