ENST00000682266.1:c.1455T>C
|
ENSP00000507766.1:p.Ala485=
|
|
ENST00000682341.1:c.1863T>C
|
ENSP00000508251.1:p.Ala621=
|
|
ENST00000683197.1:c.1863T>C
|
ENSP00000507641.1:p.Ala621=
|
|
ENST00000683411.1:c.1455T>C
|
ENSP00000508397.1:p.Ala485=
|
|
ENST00000683437.1:c.1455T>C
|
ENSP00000508408.1:p.Ala485=
|
|
ENST00000683613.1:n.2899T>C
|
|
|
ENST00000684663.1:c.1860T>C
|
ENSP00000508009.1:p.Ala620=
|
|
ENST00000324559.9:c.1905T>C
MANE Select
|
ENSP00000315371.9:p.Ala635=
|
|
ENST00000648804.1:n.2240T>C
|
|
|
ENST00000324559.8:c.1905T>C
|
ENSP00000315371.8:p.Ala635=
|
|
NM_001142649.1:c.1902T>C
|
NP_001136121.1:p.Ala634=
|
|
NM_213599.2:c.1905T>C , LRG_868t1:c.1905T>C
|
NP_998764.1:p.Ala635=
|
|
XM_005252820.2:c.1863T>C
|
XP_005252877.2:p.Ala621=
|
|
XM_005252821.2:c.1860T>C
|
XP_005252878.2:p.Ala620=
|
|
XM_005252822.3:c.1827T>C
|
XP_005252879.1:p.Ala609=
|
|
XM_005252823.3:c.1824T>C
|
XP_005252880.1:p.Ala608=
|
|
XM_011519949.1:c.1812T>C
|
XP_011518251.1:p.Ala604=
|
|
XM_005252820.3:c.1863T>C
|
XP_005252877.2:p.Ala621=
|
|
XM_005252821.3:c.1860T>C
|
XP_005252878.2:p.Ala620=
|
|
XM_005252822.4:c.1827T>C
|
XP_005252879.1:p.Ala609=
|
|
XM_011519949.2:c.1812T>C
|
XP_011518251.1:p.Ala604=
|
|
NM_001142649.2:c.1902T>C
|
NP_001136121.1:p.Ala634=
|
|
NM_213599.3:c.1905T>C
MANE Select
|
NP_998764.1:p.Ala635=
|
|