ENST00000302068.9:c.1237G>C
MANE Select
|
ENSP00000306099.4:p.Asp413His
|
|
ENST00000302068.8:c.1237G>C
|
ENSP00000306099.4:p.Asp413His
|
|
ENST00000502545.5:n.939+485G>C
|
|
|
ENST00000509493.1:c.580G>C
|
ENSP00000426757.1:p.Asp194His
|
|
NM_001184741.1:c.1060G>C
|
NP_001171670.1:p.Asp354His
|
|
NM_005141.4:c.1237G>C , LRG_558t1:c.1237G>C
|
NP_005132.2:p.Asp413His
|
|
NM_001382759.1:c.1105G>C
|
NP_001369688.1:p.Asp369His
|
|
NM_001382760.1:c.1237G>C
|
NP_001369689.1:p.Asp413His
|
|
NM_001382761.1:c.1237G>C
|
NP_001369690.1:p.Asp413His
|
|
NM_001382762.1:c.937G>C
|
NP_001369691.1:p.Asp313His
|
|
NM_001382763.1:c.1228G>C
|
NP_001369692.1:p.Asp410His
|
|
NM_001382764.1:c.*11G>C
|
NP_001369693.1:n.*11G>C
|
|
NM_001382765.1:c.1220+17G>C
|
NP_001369694.1:n.1220+17G>C
|
|
NM_005141.5:c.1237G>C
MANE Select
|
NP_005132.2:p.Asp413His
|
|