ENST00000264071.7:c.670G>C
MANE Select
|
ENSP00000264071.1:p.Asp224His
|
|
ENST00000264071.6:c.670G>C
|
ENSP00000264071.1:p.Asp224His
|
|
ENST00000540257.5:c.670G>C
|
ENSP00000443590.1:p.Asp224His
|
|
ENST00000594075.5:c.460G>C
|
ENSP00000469936.1:p.Asp154His
|
|
ENST00000594276.5:c.358G>C
|
ENSP00000472481.1:p.Asp120His
|
|
ENST00000600216.5:c.412G>C
|
ENSP00000470983.1:p.Asp138His
|
|
NM_001289123.1:c.823G>C
|
NP_001276052.1:p.Asp275His
|
|
NM_001289127.1:c.805G>C
|
NP_001276056.1:p.Asp269His
|
|
NM_001289129.1:c.670G>C
|
NP_001276058.1:p.Asp224His
|
|
NM_001289130.1:c.454G>C
|
NP_001276059.1:p.Asp152His
|
|
NM_001289131.1:c.454G>C
|
NP_001276060.1:p.Asp152His
|
|
NM_006087.3:c.670G>C
|
NP_006078.2:p.Asp224His
|
|
NM_006087.4:c.670G>C
MANE Select
|
NP_006078.2:p.Asp224His
|
|
NM_001289123.2:c.823G>C
|
NP_001276052.1:p.Asp275His
|
|
NM_001289127.2:c.805G>C
|
NP_001276056.1:p.Asp269His
|
|
NM_001289129.2:c.670G>C
|
NP_001276058.1:p.Asp224His
|
|
NM_001289130.2:c.454G>C
|
NP_001276059.1:p.Asp152His
|
|
NM_001289131.2:c.454G>C
|
NP_001276060.1:p.Asp152His
|
|