ENST00000272371.7:c.5103G>T
MANE Select
|
ENSP00000272371.2:p.Gln1701His
|
|
ENST00000339598.8:c.2802G>T
MANE Plus Clinical
|
ENSP00000344521.3:p.Gln934His
|
|
ENST00000402415.8:c.2862G>T
|
ENSP00000383906.4:p.Gln954His
|
|
ENST00000272371.6:c.5103G>T
|
ENSP00000272371.2:p.Gln1701His
|
|
ENST00000338581.10:c.2802G>T
|
ENSP00000345137.6:p.Gln934His
|
|
ENST00000339598.7:c.2802G>T
|
ENSP00000344521.3:p.Gln934His
|
|
ENST00000402415.7:c.3033G>T
|
ENSP00000383906.3:p.Gln1011His
|
|
ENST00000403946.7:c.5103G>T
|
ENSP00000385255.3:p.Gln1701His
|
|
ENST00000464574.1:n.852G>T
|
|
|
NM_001287489.1:c.5103G>T
|
NP_001274418.1:p.Gln1701His
|
|
NM_004802.3:c.2802G>T
|
NP_004793.2:p.Gln934His
|
|
NM_194248.2:c.5103G>T
|
NP_919224.1:p.Gln1701His
|
|
NM_194322.2:c.3033G>T
|
NP_919303.1:p.Gln1011His
|
|
NM_194323.2:c.2802G>T
|
NP_919304.1:p.Gln934His
|
|
XM_005264644.2:c.5088G>T
|
XP_005264701.1:p.Gln1696His
|
|
XM_011533185.1:c.5148G>T
|
XP_011531487.1:p.Gln1716His
|
|
XM_017005338.1:c.5043G>T
|
XP_016860827.1:p.Gln1681His
|
|
NM_001287489.2:c.5103G>T
|
NP_001274418.1:p.Gln1701His
|
|
NM_004802.4:c.2802G>T
|
NP_004793.2:p.Gln934His
|
|
NM_194248.3:c.5103G>T
MANE Select
|
NP_919224.1:p.Gln1701His
|
|
NM_194322.3:c.3033G>T
|
NP_919303.1:p.Gln1011His
|
|
NM_194323.3:c.2802G>T
MANE Plus Clinical
|
NP_919304.1:p.Gln934His
|
|