ENST00000368485.8:c.1367C>A
MANE Select
|
ENSP00000357470.3:p.Pro456His
|
|
ENST00000344086.8:c.*175C>A
|
ENSP00000340589.4:n.*175C>A
|
|
ENST00000368485.7:c.1367C>A
|
ENSP00000357470.3:p.Pro456His
|
|
NM_000565.3:c.1367C>A
|
NP_000556.1:p.Pro456His
|
|
NM_181359.2:c.*175C>A
|
NP_852004.1:n.*175C>A
|
|
XM_005245139.1:c.*48C>A
|
XP_005245196.1:n.*48C>A
|
|
XM_005245140.1:c.*208C>A
|
XP_005245197.1:n.*208C>A
|
|
XM_006711298.1:c.1415C>A
|
XP_006711361.1:p.Pro472His
|
|
XM_005245139.2:c.*48C>A
|
XP_005245196.1:n.*48C>A
|
|
XM_005245140.3:c.*208C>A
|
XP_005245197.1:n.*208C>A
|
|
XM_006711298.2:c.1415C>A
|
XP_006711361.1:p.Pro472His
|
|
XM_017001199.2:c.1514C>A
|
XP_016856688.1:p.Pro505His
|
|
XM_017001200.2:c.1466C>A
|
XP_016856689.1:p.Pro489His
|
|
XM_017001201.2:c.*208C>A
|
XP_016856690.1:n.*208C>A
|
|
NM_000565.4:c.1367C>A
MANE Select
|
NP_000556.1:p.Pro456His
|
|
NM_181359.3:c.*175C>A
|
NP_852004.1:n.*175C>A
|
|
NM_001382769.1:c.1466C>A
|
NP_001369698.1:p.Pro489His
|
|
NM_001382770.1:c.1460C>A
|
NP_001369699.1:p.Pro487His
|
|
NM_001382771.1:c.1415C>A
|
NP_001369700.1:p.Pro472His
|
|
NM_001382772.1:c.1361C>A
|
NP_001369701.1:p.Pro454His
|
|
NM_001382773.1:c.*175C>A
|
NP_001369702.1:n.*175C>A
|
|
NM_001382774.1:c.1007C>A
|
NP_001369703.1:p.Pro336His
|
|