|
ENST00000326735.13:c.1252A>C
MANE Select
|
ENSP00000327214.8:p.Asn418His
|
|
|
ENST00000326735.12:c.1252A>C
|
ENSP00000327214.8:p.Asn418His
|
|
|
ENST00000341676.9:c.1237A>C
|
ENSP00000341115.5:p.Asn413His
|
|
|
ENST00000452699.5:c.1237A>C
|
ENSP00000413307.1:p.Asn413His
|
|
|
ENST00000463860.5:n.860A>C
|
|
|
|
ENST00000502860.1:n.335-140A>C
|
|
|
|
ENST00000506174.5:c.394A>C
|
ENSP00000424393.1:p.Asn132His
|
|
|
ENST00000509392.1:n.255A>C
|
|
|
|
ENST00000617114.4:c.335-140A>C
|
ENSP00000478781.1:n.335-140A>C
|
|
|
NM_001141973.2:c.1237A>C
|
NP_001135445.1:p.Asn413His
|
|
|
NM_001141974.2:c.1237A>C
|
NP_001135446.1:p.Asn413His
|
|
|
NM_022089.3:c.1252A>C
|
NP_071372.1:p.Asn418His
|
|
|
XM_005245809.1:c.1252A>C
|
XP_005245866.1:p.Asn418His
|
|
|
XM_005245810.1:c.1249A>C
|
XP_005245867.1:p.Asn417His
|
|
|
XM_005245811.1:c.1237A>C
|
XP_005245868.1:p.Asn413His
|
|
|
XM_005245812.1:c.1225A>C
|
XP_005245869.1:p.Asn409His
|
|
|
XM_005245813.1:c.1252A>C
|
XP_005245870.1:p.Asn418His
|
|
|
XM_005245815.1:c.1252A>C
|
XP_005245872.1:p.Asn418His
|
|
|
XM_006710512.1:c.1234A>C
|
XP_006710575.1:p.Asn412His
|
|
|
XM_006710513.1:c.1210A>C
|
XP_006710576.1:p.Asn404His
|
|
|
XM_011541128.1:c.1252A>C
|
XP_011539430.1:p.Asn418His
|
|
|
XM_011541129.1:c.1252A>C
|
XP_011539431.1:p.Asn418His
|
|
|
XM_017000844.1:c.1252A>C
|
XP_016856333.1:p.Asn418His
|
|
|
XM_017000845.1:c.1234A>C
|
XP_016856334.1:p.Asn412His
|
|
|
XM_017000846.1:c.1210A>C
|
XP_016856335.1:p.Asn404His
|
|
|
XM_017000847.1:c.1222A>C
|
XP_016856336.1:p.Asn408His
|
|
|
XM_017000848.1:c.1252A>C
|
XP_016856337.1:p.Asn418His
|
|
|
XM_017000849.1:c.1237A>C
|
XP_016856338.1:p.Asn413His
|
|
|
XM_017000850.1:c.1252A>C
|
XP_016856339.1:p.Asn418His
|
|
|
NM_022089.4:c.1252A>C
MANE Select
|
NP_071372.1:p.Asn418His
|
|
|
NM_001141973.3:c.1237A>C
|
NP_001135445.1:p.Asn413His
|
|
|
NM_001141974.3:c.1237A>C
|
NP_001135446.1:p.Asn413His
|
|
