ENST00000302068.9:c.1222T>C
MANE Select
|
ENSP00000306099.4:p.Tyr408His
|
|
ENST00000302068.8:c.1222T>C
|
ENSP00000306099.4:p.Tyr408His
|
|
ENST00000502545.5:n.939+470T>C
|
|
|
ENST00000509493.1:c.565T>C
|
ENSP00000426757.1:p.Tyr189His
|
|
NM_001184741.1:c.1045T>C
|
NP_001171670.1:p.Tyr349His
|
|
NM_005141.4:c.1222T>C , LRG_558t1:c.1222T>C
|
NP_005132.2:p.Tyr408His
|
|
NM_001382759.1:c.1090T>C
|
NP_001369688.1:p.Tyr364His
|
|
NM_001382760.1:c.1222T>C
|
NP_001369689.1:p.Tyr408His
|
|
NM_001382761.1:c.1222T>C
|
NP_001369690.1:p.Tyr408His
|
|
NM_001382762.1:c.922T>C
|
NP_001369691.1:p.Tyr308His
|
|
NM_001382763.1:c.1213T>C
|
NP_001369692.1:p.Tyr405His
|
|
NM_001382764.1:c.1085T>C
|
NP_001369693.1:p.Val362Ala
|
|
NM_001382765.1:c.1220+2T>C
|
NP_001369694.1:n.1220+2T>C
|
|
NM_005141.5:c.1222T>C
MANE Select
|
NP_005132.2:p.Tyr408His
|
|