ENST00000389054.8:c.2067A>C
MANE Select
|
ENSP00000373706.4:p.Pro689=
|
|
ENST00000647433.1:c.2067A>C
|
ENSP00000494675.1:p.Pro689=
|
|
ENST00000253811.10:c.1935A>C
|
ENSP00000253811.7:p.Pro645=
|
|
ENST00000389054.7:c.2067A>C
|
ENSP00000373706.4:p.Pro689=
|
|
ENST00000389057.9:c.2040A>C
|
ENSP00000373709.6:p.Pro680=
|
|
ENST00000398557.8:c.2067A>C
|
ENSP00000381565.5:p.Pro689=
|
|
ENST00000518047.5:c.2040A>C
|
ENSP00000428268.2:p.Pro680=
|
|
NM_001079812.2:c.2040A>C
|
NP_001073280.1:p.Pro680=
|
|
NM_001314007.1:c.2067A>C
|
NP_001300936.1:p.Pro689=
|
|
NM_005219.4:c.2067A>C
|
NP_005210.3:p.Pro689=
|
|
XM_011537572.1:c.2031A>C
|
XP_011535874.1:p.Pro677=
|
|
XM_011537573.1:c.2001A>C
|
XP_011535875.1:p.Pro667=
|
|
XM_024454384.1:c.2067A>C
|
XP_024310152.1:p.Pro689=
|
|
XM_024454385.1:c.2040A>C
|
XP_024310153.1:p.Pro680=
|
|
XM_024454386.1:c.2031A>C
|
XP_024310154.1:p.Pro677=
|
|
XM_024454387.1:c.2001A>C
|
XP_024310155.1:p.Pro667=
|
|
NM_005219.5:c.2067A>C
MANE Select
|
NP_005210.3:p.Pro689=
|
|
NM_001079812.3:c.2040A>C
|
NP_001073280.1:p.Pro680=
|
|
NM_001314007.2:c.2067A>C
|
NP_001300936.1:p.Pro689=
|
|