ENST00000368485.8:c.1243C>G
MANE Select
|
ENSP00000357470.3:p.Pro415Ala
|
|
ENST00000344086.8:c.*51C>G
|
ENSP00000340589.4:n.*51C>G
|
|
ENST00000368485.7:c.1243C>G
|
ENSP00000357470.3:p.Pro415Ala
|
|
ENST00000502679.1:n.556C>G
|
|
|
ENST00000507256.1:n.441C>G
|
|
|
NM_000565.3:c.1243C>G
|
NP_000556.1:p.Pro415Ala
|
|
NM_181359.2:c.*51C>G
|
NP_852004.1:n.*51C>G
|
|
XM_005245139.1:c.1007C>G
|
XP_005245196.1:p.Pro336Arg
|
|
XM_005245140.1:c.*84C>G
|
XP_005245197.1:n.*84C>G
|
|
XM_006711298.1:c.1291C>G
|
XP_006711361.1:p.Pro431Ala
|
|
XM_006711299.2:c.*51C>G
|
XP_006711362.1:n.*51C>G
|
|
XM_005245139.2:c.1007C>G
|
XP_005245196.1:p.Pro336Arg
|
|
XM_005245140.3:c.*84C>G
|
XP_005245197.1:n.*84C>G
|
|
XM_006711298.2:c.1291C>G
|
XP_006711361.1:p.Pro431Ala
|
|
XM_006711299.4:c.*51C>G
|
XP_006711362.1:n.*51C>G
|
|
XM_017001199.2:c.1390C>G
|
XP_016856688.1:p.Pro464Ala
|
|
XM_017001200.2:c.1342C>G
|
XP_016856689.1:p.Pro448Ala
|
|
XM_017001201.2:c.*84C>G
|
XP_016856690.1:n.*84C>G
|
|
NM_000565.4:c.1243C>G
MANE Select
|
NP_000556.1:p.Pro415Ala
|
|
NM_181359.3:c.*51C>G
|
NP_852004.1:n.*51C>G
|
|
NM_001382769.1:c.1342C>G
|
NP_001369698.1:p.Pro448Ala
|
|
NM_001382770.1:c.1336C>G
|
NP_001369699.1:p.Pro446Ala
|
|
NM_001382771.1:c.1291C>G
|
NP_001369700.1:p.Pro431Ala
|
|
NM_001382772.1:c.1237C>G
|
NP_001369701.1:p.Pro413Ala
|
|
NM_001382773.1:c.*51C>G
|
NP_001369702.1:n.*51C>G
|
|
NM_001382774.1:c.883C>G
|
NP_001369703.1:p.Pro295Ala
|
|