ENST00000371270.6:c.1315G>A
MANE Select
|
ENSP00000360317.3:p.Gly439Arg
|
|
ENST00000371270.5:c.1315G>A
|
ENSP00000360317.3:p.Gly439Arg
|
|
ENST00000490994.6:c.*1101G>A
|
ENSP00000433314.1:n.*1101G>A
|
|
ENST00000525991.5:c.*890G>A
|
ENSP00000433842.1:n.*890G>A
|
|
ENST00000526814.5:n.1570G>A
|
|
|
ENST00000527420.5:c.*172G>A
|
ENSP00000433191.1:n.*172G>A
|
|
ENST00000527953.5:n.1609G>A
|
|
|
ENST00000531714.1:n.503G>A
|
|
|
ENST00000533320.5:n.1549G>A
|
|
|
ENST00000535898.5:c.1009G>A
|
ENSP00000445062.1:p.Gly337Arg
|
|
ENST00000539050.5:c.1105G>A
|
ENSP00000442343.2:p.Gly369Arg
|
|
ENST00000623108.3:c.1105G>A
|
ENSP00000485110.1:p.Gly369Arg
|
|
NM_000770.3:c.1315G>A
MANE Select
|
NP_000761.3:p.Gly439Arg
|
|
NM_001198853.1:c.1105G>A
|
NP_001185782.1:p.Gly369Arg
|
|
NM_001198854.1:c.1009G>A
|
NP_001185783.1:p.Gly337Arg
|
|
NM_001198855.1:c.1105G>A
|
NP_001185784.1:p.Gly369Arg
|
|
XR_945610.1:n.1450G>A
|
|
|