|
ENST00000330513.10:c.209G>A
|
ENSP00000327959.6:p.Arg70His
|
|
|
ENST00000343820.10:c.269G>A
MANE Select
|
ENSP00000339631.6:p.Arg90His
|
|
|
ENST00000330513.9:c.656G>A
|
ENSP00000327959.5:p.Arg219His
|
|
|
ENST00000343820.9:c.269G>A
|
ENSP00000339631.5:p.Arg90His
|
|
|
ENST00000345133.9:c.209G>A
|
ENSP00000343969.5:p.Arg70His
|
|
|
ENST00000400167.6:c.209G>A
|
ENSP00000383031.2:p.Arg70His
|
|
|
ENST00000401449.5:c.209G>A
|
ENSP00000385206.1:p.Arg70His
|
|
|
ENST00000405385.7:c.209G>A
|
ENSP00000384970.2:p.Arg70His
|
|
|
ENST00000407501.6:c.269G>A
|
ENSP00000384133.2:p.Arg90His
|
|
|
ENST00000472042.1:c.209G>A
|
ENSP00000449501.1:p.Arg70His
|
|
|
ENST00000546979.5:c.269G>A
|
ENSP00000448934.1:p.Arg90His
|
|
|
ENST00000548489.6:c.209G>A
|
ENSP00000447747.2:p.Arg70His
|
|
|
ENST00000549253.5:c.209G>A
|
ENSP00000449973.1:p.Arg70His
|
|
|
ENST00000549468.5:c.209G>A
|
ENSP00000449722.1:p.Arg70His
|
|
|
ENST00000549546.5:c.209G>A
|
ENSP00000449580.1:p.Arg70His
|
|
|
ENST00000549780.5:c.209G>A
|
ENSP00000448121.1:p.Arg70His
|
|
|
ENST00000550958.5:c.209G>A
|
ENSP00000449531.1:p.Arg70His
|
|
|
ENST00000551333.1:c.209G>A
|
ENSP00000446838.1:p.Arg70His
|
|
|
ENST00000551541.5:c.209G>A
|
ENSP00000450025.1:p.Arg70His
|
|
|
ENST00000552383.5:c.209G>A
|
ENSP00000449287.1:p.Arg70His
|
|
|
ENST00000577543.5:c.244-7G>A
|
ENSP00000462285.1:n.244-7G>A
|
|
|
ENST00000618001.4:c.311G>A
|
ENSP00000483499.1:p.Arg104His
|
|
|
NM_001278682.1:c.278G>A
|
NP_001265611.1:p.Arg93His
|
|
|
NM_001278684.1:c.269G>A
|
NP_001265613.1:p.Arg90His
|
|
|
NM_001278686.1:c.209G>A
|
NP_001265615.1:p.Arg70His
|
|
|
NM_003244.3:c.269G>A
|
NP_003235.1:p.Arg90His
|
|
|
NM_170695.3:c.656G>A
|
NP_733796.2:p.Arg219His
|
|
|
NM_173207.2:c.311G>A
|
NP_775299.1:p.Arg104His
|
|
|
NM_173208.2:c.269G>A
|
NP_775300.1:p.Arg90His
|
|
|
NM_173209.2:c.209G>A
|
NP_775301.1:p.Arg70His
|
|
|
NM_173210.2:c.209G>A
|
NP_775302.1:p.Arg70His
|
|
|
NM_173211.1:c.209G>A
|
NP_775303.1:p.Arg70His
|
|
|
NM_174886.2:c.209G>A
|
NP_777480.1:p.Arg70His
|
|
|
XM_011525735.1:c.209G>A
|
XP_011524037.1:p.Arg70His
|
|
|
XM_011525735.2:c.209G>A
|
XP_011524037.1:p.Arg70His
|
|
|
XM_017025958.1:c.269G>A
|
XP_016881447.1:p.Arg90His
|
|
|
XM_017025959.1:c.209G>A
|
XP_016881448.1:p.Arg70His
|
|
|
NM_001278682.2:c.278G>A
|
NP_001265611.1:p.Arg93His
|
|
|
NM_001278684.2:c.269G>A
|
NP_001265613.1:p.Arg90His
|
|
|
NM_001278686.2:c.209G>A
|
NP_001265615.1:p.Arg70His
|
|
|
NM_001374396.1:c.209G>A
|
NP_001361325.1:p.Arg70His
|
|
|
NM_001374397.1:c.209G>A
|
NP_001361326.1:p.Arg70His
|
|
|
NM_003244.4:c.269G>A
MANE Select
|
NP_003235.1:p.Arg90His
|
|
|
NM_170695.5:c.209G>A
|
NP_733796.3:p.Arg70His
|
|
|
NM_173207.4:c.311G>A
|
NP_775299.1:p.Arg104His
|
|
|
NM_173208.3:c.269G>A
|
NP_775300.1:p.Arg90His
|
|
|
NM_173209.3:c.209G>A
|
NP_775301.1:p.Arg70His
|
|
|
NM_173210.4:c.209G>A
|
NP_775302.1:p.Arg70His
|
|
|
NM_173211.2:c.209G>A
|
NP_775303.1:p.Arg70His
|
|
|
NM_174886.3:c.209G>A
|
NP_777480.1:p.Arg70His
|
|
|
NM_001278686.3:c.209G>A
|
NP_001265615.1:p.Arg70His
|
|
