ENST00000368485.8:c.1366C>G
MANE Select
|
ENSP00000357470.3:p.Pro456Ala
|
|
ENST00000344086.8:c.*174C>G
|
ENSP00000340589.4:n.*174C>G
|
|
ENST00000368485.7:c.1366C>G
|
ENSP00000357470.3:p.Pro456Ala
|
|
NM_000565.3:c.1366C>G
|
NP_000556.1:p.Pro456Ala
|
|
NM_181359.2:c.*174C>G
|
NP_852004.1:n.*174C>G
|
|
XM_005245139.1:c.*47C>G
|
XP_005245196.1:n.*47C>G
|
|
XM_005245140.1:c.*207C>G
|
XP_005245197.1:n.*207C>G
|
|
XM_006711298.1:c.1414C>G
|
XP_006711361.1:p.Pro472Ala
|
|
XM_005245139.2:c.*47C>G
|
XP_005245196.1:n.*47C>G
|
|
XM_005245140.3:c.*207C>G
|
XP_005245197.1:n.*207C>G
|
|
XM_006711298.2:c.1414C>G
|
XP_006711361.1:p.Pro472Ala
|
|
XM_017001199.2:c.1513C>G
|
XP_016856688.1:p.Pro505Ala
|
|
XM_017001200.2:c.1465C>G
|
XP_016856689.1:p.Pro489Ala
|
|
XM_017001201.2:c.*207C>G
|
XP_016856690.1:n.*207C>G
|
|
NM_000565.4:c.1366C>G
MANE Select
|
NP_000556.1:p.Pro456Ala
|
|
NM_181359.3:c.*174C>G
|
NP_852004.1:n.*174C>G
|
|
NM_001382769.1:c.1465C>G
|
NP_001369698.1:p.Pro489Ala
|
|
NM_001382770.1:c.1459C>G
|
NP_001369699.1:p.Pro487Ala
|
|
NM_001382771.1:c.1414C>G
|
NP_001369700.1:p.Pro472Ala
|
|
NM_001382772.1:c.1360C>G
|
NP_001369701.1:p.Pro454Ala
|
|
NM_001382773.1:c.*174C>G
|
NP_001369702.1:n.*174C>G
|
|
NM_001382774.1:c.1006C>G
|
NP_001369703.1:p.Pro336Ala
|
|