ENST00000302068.9:c.1221G>T
MANE Select
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ENSP00000306099.4:p.Thr407=
|
|
ENST00000302068.8:c.1221G>T
|
ENSP00000306099.4:p.Thr407=
|
|
ENST00000502545.5:n.939+469G>T
|
|
|
ENST00000509493.1:c.564G>T
|
ENSP00000426757.1:p.Thr188=
|
|
NM_001184741.1:c.1044G>T
|
NP_001171670.1:p.Thr348=
|
|
NM_005141.4:c.1221G>T , LRG_558t1:c.1221G>T
|
NP_005132.2:p.Thr407=
|
|
NM_001382759.1:c.1089G>T
|
NP_001369688.1:p.Thr363=
|
|
NM_001382760.1:c.1221G>T
|
NP_001369689.1:p.Thr407=
|
|
NM_001382761.1:c.1221G>T
|
NP_001369690.1:p.Thr407=
|
|
NM_001382762.1:c.921G>T
|
NP_001369691.1:p.Thr307=
|
|
NM_001382763.1:c.1212G>T
|
NP_001369692.1:p.Thr404=
|
|
NM_001382764.1:c.1084G>T
|
NP_001369693.1:p.Val362Leu
|
|
NM_001382765.1:c.1220+1G>T
|
NP_001369694.1:n.1220+1G>T
|
|
NM_005141.5:c.1221G>T
MANE Select
|
NP_005132.2:p.Thr407=
|
|