ENST00000371270.6:c.1325G>A
MANE Select
|
ENSP00000360317.3:p.Arg442His
|
|
ENST00000371270.5:c.1325G>A
|
ENSP00000360317.3:p.Arg442His
|
|
ENST00000490994.6:c.*1111G>A
|
ENSP00000433314.1:n.*1111G>A
|
|
ENST00000525991.5:c.*900G>A
|
ENSP00000433842.1:n.*900G>A
|
|
ENST00000526814.5:n.1580G>A
|
|
|
ENST00000527420.5:c.*182G>A
|
ENSP00000433191.1:n.*182G>A
|
|
ENST00000527953.5:n.1619G>A
|
|
|
ENST00000531714.1:n.513G>A
|
|
|
ENST00000533320.5:n.1559G>A
|
|
|
ENST00000535898.5:c.1019G>A
|
ENSP00000445062.1:p.Arg340His
|
|
ENST00000539050.5:c.1115G>A
|
ENSP00000442343.2:p.Arg372His
|
|
ENST00000623108.3:c.1115G>A
|
ENSP00000485110.1:p.Arg372His
|
|
NM_000770.3:c.1325G>A
MANE Select
|
NP_000761.3:p.Arg442His
|
|
NM_001198853.1:c.1115G>A
|
NP_001185782.1:p.Arg372His
|
|
NM_001198854.1:c.1019G>A
|
NP_001185783.1:p.Arg340His
|
|
NM_001198855.1:c.1115G>A
|
NP_001185784.1:p.Arg372His
|
|
XR_945610.1:n.1460G>A
|
|
|