|
ENST00000460011.6:c.-122T>C
|
ENSP00000507070.1:n.-122T>C
|
|
|
ENST00000494498.2:c.77T>C
|
ENSP00000507847.1:p.Val26Ala
|
|
|
ENST00000397746.8:c.1343T>C
MANE Select
|
ENSP00000380854.3:p.Val448Ala
|
|
|
ENST00000291670.9:c.1343T>C
|
ENSP00000291670.5:p.Val448Ala
|
|
|
ENST00000397743.1:c.1299T>C
|
ENSP00000380851.1:p.Ser433=
|
|
|
ENST00000397746.7:c.1343T>C
|
ENSP00000380854.3:p.Val448Ala
|
|
|
ENST00000397748.5:c.1343T>C
|
ENSP00000380856.1:p.Val448Ala
|
|
|
ENST00000460011.5:n.672T>C
|
|
|
|
ENST00000488577.1:n.369T>C
|
|
|
|
ENST00000494498.1:n.644T>C
|
|
|
|
ENST00000498355.6:n.1412T>C
|
|
|
|
NM_006657.2:c.1343T>C
|
NP_006648.1:p.Val448Ala
|
|
|
NM_206965.1:c.1343T>C
|
NP_996848.1:p.Val448Ala
|
|
|
XM_006723961.2:c.1592T>C
|
XP_006724024.2:p.Val531Ala
|
|
|
XM_006723962.2:c.1592T>C
|
XP_006724025.2:p.Val531Ala
|
|
|
XM_011529434.1:c.1592T>C
|
XP_011527736.1:p.Val531Ala
|
|
|
XM_011529435.1:c.1463T>C
|
XP_011527737.1:p.Val488Ala
|
|
|
XM_011529436.1:c.1592T>C
|
XP_011527738.1:p.Val531Ala
|
|
|
XM_011529437.1:c.1592T>C
|
XP_011527739.1:p.Val531Ala
|
|
|
XM_011529438.1:c.1463T>C
|
XP_011527740.1:p.Val488Ala
|
|
|
XM_011529439.1:c.1079T>C
|
XP_011527741.1:p.Val360Ala
|
|
|
XR_937433.1:n.1775T>C
|
|
|
|
NM_001320412.1:c.1343T>C
|
NP_001307341.1:p.Val448Ala
|
|
|
XM_006723961.4:c.1592T>C
|
XP_006724024.2:p.Val531Ala
|
|
|
XM_006723962.4:c.1592T>C
|
XP_006724025.2:p.Val531Ala
|
|
|
XM_011529434.3:c.1592T>C
|
XP_011527736.1:p.Val531Ala
|
|
|
XM_011529435.3:c.1463T>C
|
XP_011527737.1:p.Val488Ala
|
|
|
XM_011529436.3:c.1592T>C
|
XP_011527738.1:p.Val531Ala
|
|
|
XM_011529437.3:c.1592T>C
|
XP_011527739.1:p.Val531Ala
|
|
|
XM_011529439.2:c.1079T>C
|
XP_011527741.1:p.Val360Ala
|
|
|
XR_937433.3:n.1809T>C
|
|
|
|
NM_206965.2:c.1343T>C
MANE Select
|
NP_996848.1:p.Val448Ala
|
|
|
NM_001320412.2:c.1343T>C
|
NP_001307341.1:p.Val448Ala
|
|
|
NM_006657.3:c.1343T>C
|
NP_006648.1:p.Val448Ala
|
|
