ENST00000490131.7:c.2441G>A
|
ENSP00000418685.2:p.Arg814His
|
|
ENST00000498619.4:c.2702G>A
|
ENSP00000420194.1:p.Arg901His
|
|
ENST00000638421.1:c.2672G>A
|
ENSP00000492190.1:p.Arg891His
|
|
ENST00000639785.2:c.2672G>A
MANE Select
|
ENSP00000491584.2:p.Arg891His
|
|
ENST00000490131.5:c.2672G>A
|
ENSP00000418685.1:p.Arg891His
|
|
ENST00000498619.2:c.2702G>A
|
ENSP00000420194.1:p.Arg901His
|
|
NM_000388.3:c.2672G>A
|
NP_000379.2:p.Arg891His
|
|
NM_001178065.1:c.2702G>A
|
NP_001171536.1:p.Arg901His
|
|
XM_005247836.2:c.2672G>A
|
XP_005247893.1:p.Arg891His
|
|
XM_005247837.2:c.2189G>A
|
XP_005247894.1:p.Arg730His
|
|
XM_006713789.2:c.2672G>A
|
XP_006713852.1:p.Arg891His
|
|
XM_011513237.1:c.2672G>A
|
XP_011511539.1:p.Arg891His
|
|
XM_011513238.1:c.2672G>A
|
XP_011511540.1:p.Arg891His
|
|
XM_011513239.1:c.2084G>A
|
XP_011511541.1:p.Arg695His
|
|
XM_006713789.3:c.2672G>A
|
XP_006713852.1:p.Arg891His
|
|
XM_017007324.1:c.2672G>A
|
XP_016862813.1:p.Arg891His
|
|
XM_017007325.1:c.2672G>A
|
XP_016862814.1:p.Arg891His
|
|
NM_000388.4:c.2672G>A
MANE Select
|
NP_000379.3:p.Arg891His
|
|
NM_001178065.2:c.2702G>A
|
NP_001171536.2:p.Arg901His
|
|