|
ENST00000340107.9:c.1882A>G
|
ENSP00000339824.4:p.Thr628Ala
|
|
|
ENST00000260795.8:c.*932A>G
|
ENSP00000260795.3:n.*932A>G
|
|
|
ENST00000352904.6:c.1540A>G
|
ENSP00000231803.1:p.Thr514Ala
|
|
|
ENST00000412135.7:c.1864A>G
|
ENSP00000412903.3:p.Thr622Ala
|
|
|
ENST00000440486.8:c.1876A>G
MANE Select
|
ENSP00000414914.2:p.Thr626Ala
|
|
|
ENST00000481110.7:c.1879A>G
|
ENSP00000420533.2:p.Thr627Ala
|
|
|
ENST00000260795.6:c.1876A>G
|
ENSP00000260795.2:p.Thr626Ala
|
|
|
ENST00000340107.8:c.1882A>G
|
ENSP00000339824.4:p.Thr628Ala
|
|
|
ENST00000352904.5:c.1540A>G
|
ENSP00000231803.1:p.Thr514Ala
|
|
|
ENST00000412135.6:c.1540A>G
|
ENSP00000412903.2:p.Thr514Ala
|
|
|
ENST00000440486.6:c.1876A>G
|
ENSP00000414914.2:p.Thr626Ala
|
|
|
ENST00000481110.6:c.1879A>G
|
ENSP00000420533.2:p.Thr627Ala
|
|
|
ENST00000613647.4:c.*932A>G
|
ENSP00000479472.1:n.*932A>G
|
|
|
NM_000142.4:c.1876A>G , LRG_1021t1:c.1876A>G
|
NP_000133.1:p.Thr626Ala
|
|
|
NM_001163213.1:c.1882A>G , LRG_1021t2:c.1882A>G
|
NP_001156685.1:p.Thr628Ala
|
|
|
NM_022965.3:c.1540A>G
|
NP_075254.1:p.Thr514Ala
|
|
|
XM_006713868.1:c.1888A>G
|
XP_006713931.1:p.Thr630Ala
|
|
|
XM_006713869.1:c.1888A>G
|
XP_006713932.1:p.Thr630Ala
|
|
|
XM_006713870.1:c.1885A>G
|
XP_006713933.1:p.Thr629Ala
|
|
|
XM_006713871.1:c.1882A>G
|
XP_006713934.1:p.Thr628Ala
|
|
|
XM_006713872.1:c.1879A>G
|
XP_006713935.1:p.Thr627Ala
|
|
|
XM_006713873.1:c.1876A>G
|
XP_006713936.1:p.Thr626Ala
|
|
|
XM_011513420.1:c.1882A>G
|
XP_011511722.1:p.Thr628Ala
|
|
|
XM_011513422.1:c.1879A>G
|
XP_011511724.1:p.Thr627Ala
|
|
|
NM_001354809.1:c.1879A>G
|
NP_001341738.1:p.Thr627Ala
|
|
|
NM_001354810.1:c.1879A>G
|
NP_001341739.1:p.Thr627Ala
|
|
|
NR_148971.1:n.2283A>G
|
|
|
|
NM_001354809.2:c.1879A>G
|
NP_001341738.1:p.Thr627Ala
|
|
|
NM_001354810.2:c.1879A>G
|
NP_001341739.1:p.Thr627Ala
|
|
|
NR_148971.2:n.2302A>G
|
|
|
|
NM_000142.5:c.1876A>G
MANE Select
|
NP_000133.1:p.Thr626Ala
|
|
|
NM_001163213.2:c.1882A>G
|
NP_001156685.1:p.Thr628Ala
|
|
|
NM_022965.4:c.1540A>G
|
NP_075254.1:p.Thr514Ala
|
|
