|
ENST00000264731.8:c.953G>A
MANE Select
|
ENSP00000264731.3:p.Arg318His
|
|
|
ENST00000354600.10:c.671G>A
MANE Plus Clinical
|
ENSP00000346614.5:p.Arg224His
|
|
|
ENST00000264731.7:c.953G>A
|
ENSP00000264731.3:p.Arg318His
|
|
|
ENST00000320472.9:c.953G>A
|
ENSP00000317510.5:p.Arg318His
|
|
|
ENST00000354600.9:c.671G>A
|
ENSP00000346614.5:p.Arg224His
|
|
|
ENST00000392460.7:c.953G>A
|
ENSP00000376253.3:p.Arg318His
|
|
|
ENST00000392461.7:c.671G>A
|
ENSP00000376254.3:p.Arg224His
|
|
|
ENST00000392463.6:c.671G>A
|
ENSP00000376256.2:p.Arg224His
|
|
|
ENST00000418709.6:c.953G>A
|
ENSP00000407144.2:p.Arg318His
|
|
|
ENST00000437221.5:c.671G>A
|
ENSP00000392488.1:p.Arg224His
|
|
|
ENST00000440651.6:c.953G>A
|
ENSP00000394337.2:p.Arg318His
|
|
|
ENST00000449992.5:c.416G>A
|
ENSP00000387839.1:p.Arg139His
|
|
|
ENST00000456148.1:c.671G>A
|
ENSP00000389485.1:p.Arg224His
|
|
|
ENST00000460036.1:n.777G>A
|
|
|
|
NM_001114978.1:c.953G>A
|
NP_001108450.1:p.Arg318His
|
|
|
NM_001114979.1:c.953G>A
|
NP_001108451.1:p.Arg318His
|
|
|
NM_001114980.1:c.671G>A
|
NP_001108452.1:p.Arg224His
|
|
|
NM_001114981.1:c.671G>A
|
NP_001108453.1:p.Arg224His
|
|
|
NM_001114982.1:c.671G>A
|
NP_001108454.1:p.Arg224His
|
|
|
NM_003722.4:c.953G>A
|
NP_003713.3:p.Arg318His
|
|
|
XM_005247843.2:c.953G>A
|
XP_005247900.1:p.Arg318His
|
|
|
XM_005247844.3:c.902G>A
|
XP_005247901.1:p.Arg301His
|
|
|
XM_005247846.2:c.953G>A
|
XP_005247903.1:p.Arg318His
|
|
|
XM_011513251.1:c.950G>A
|
XP_011511553.1:p.Arg317His
|
|
|
XM_011513252.1:c.947G>A
|
XP_011511554.1:p.Arg316His
|
|
|
XM_011513253.1:c.914G>A
|
XP_011511555.1:p.Arg305His
|
|
|
NM_001329144.1:c.953G>A
|
NP_001316073.1:p.Arg318His
|
|
|
NM_001329145.1:c.671G>A
|
NP_001316074.1:p.Arg224His
|
|
|
NM_001329146.1:c.416G>A
|
NP_001316075.1:p.Arg139His
|
|
|
NM_001329148.1:c.953G>A
|
NP_001316077.1:p.Arg318His
|
|
|
NM_001329149.1:c.671G>A
|
NP_001316078.1:p.Arg224His
|
|
|
NM_001329150.1:c.416G>A
|
NP_001316079.1:p.Arg139His
|
|
|
NM_001329964.1:c.947G>A
|
NP_001316893.1:p.Arg316His
|
|
|
NM_003722.5:c.953G>A
MANE Select
|
NP_003713.3:p.Arg318His
|
|
|
NM_001114978.2:c.953G>A
|
NP_001108450.1:p.Arg318His
|
|
|
NM_001114979.2:c.953G>A
|
NP_001108451.1:p.Arg318His
|
|
|
NM_001114980.2:c.671G>A
MANE Plus Clinical
|
NP_001108452.1:p.Arg224His
|
|
|
NM_001114981.2:c.671G>A
|
NP_001108453.1:p.Arg224His
|
|
|
NM_001114982.2:c.671G>A
|
NP_001108454.1:p.Arg224His
|
|
|
NM_001329144.2:c.953G>A
|
NP_001316073.1:p.Arg318His
|
|
|
NM_001329145.2:c.671G>A
|
NP_001316074.1:p.Arg224His
|
|
|
NM_001329146.2:c.416G>A
|
NP_001316075.1:p.Arg139His
|
|
|
NM_001329148.2:c.953G>A
|
NP_001316077.1:p.Arg318His
|
|
|
NM_001329149.2:c.671G>A
|
NP_001316078.1:p.Arg224His
|
|
|
NM_001329150.2:c.416G>A
|
NP_001316079.1:p.Arg139His
|
|
|
NM_001329964.2:c.947G>A
|
NP_001316893.1:p.Arg316His
|
|
