ENST00000697149.1:c.1678A>C
|
ENSP00000513138.1:n.1678A>C
|
|
ENST00000697150.1:c.1736A>C
|
ENSP00000513139.1:n.1736A>C
|
|
ENST00000697151.1:c.1669A>C
|
ENSP00000513140.1:n.1669A>C
|
|
ENST00000697164.1:c.1749A>C
|
ENSP00000513153.1:p.Pro583=
|
|
ENST00000697165.1:c.1536A>C
|
ENSP00000513154.1:p.Pro512=
|
|
ENST00000347310.10:c.1839A>C
MANE Select
|
ENSP00000321345.5:p.Pro613=
|
|
ENST00000637002.1:c.1230A>C
|
ENSP00000490340.1:p.Pro410=
|
|
ENST00000347310.9:c.1839A>C
|
ENSP00000321345.5:p.Pro613=
|
|
ENST00000395227.2:c.633A>C
|
ENSP00000378652.2:p.Pro211=
|
|
ENST00000425614.3:c.1074A>C
|
ENSP00000387640.2:p.Pro358=
|
|
ENST00000473881.2:c.*665A>C
|
ENSP00000486667.1:n.*665A>C
|
|
NM_144701.2:c.1839A>C
|
NP_653302.2:p.Pro613=
|
|
XM_005270516.2:c.1077A>C
|
XP_005270573.1:p.Pro359=
|
|
XM_011540789.1:c.1929A>C
|
XP_011539091.1:p.Pro643=
|
|
XM_011540790.1:c.1839A>C
|
XP_011539092.1:p.Pro613=
|
|
XM_011540791.1:c.1839A>C
|
XP_011539093.1:p.Pro613=
|
|
XM_011540790.3:c.1839A>C
|
XP_011539092.1:p.Pro613=
|
|
XM_011540791.3:c.1839A>C
|
XP_011539093.1:p.Pro613=
|
|
XR_001736993.1:n.1919A>C
|
|
|
NM_144701.3:c.1839A>C
MANE Select
|
NP_653302.2:p.Pro613=
|
|