ENST00000348974.5:c.592G>C
|
ENSP00000330021.7:p.Asp198His
|
|
ENST00000394236.9:c.592G>C
MANE Select
|
ENSP00000377783.3:p.Asp198His
|
|
ENST00000407433.6:c.556+36G>C
|
ENSP00000385794.2:n.556+36G>C
|
|
ENST00000647936.1:c.592G>C
|
ENSP00000496822.1:p.Asp198His
|
|
ENST00000648381.1:n.760G>C
|
|
|
ENST00000648853.1:c.550G>C
|
ENSP00000497262.1:p.Asp184His
|
|
ENST00000649103.1:c.691G>C
|
ENSP00000497962.1:n.691G>C
|
|
ENST00000650591.1:c.688G>C
|
ENSP00000497376.1:p.Asp230His
|
|
ENST00000348974.4:c.688G>C
|
ENSP00000330021.6:p.Asp230His
|
|
ENST00000394236.7:c.592G>C
|
ENSP00000377783.3:p.Asp198His
|
|
ENST00000407433.5:c.199G>C
|
ENSP00000385794.1:p.Asp67His
|
|
NM_000313.3:c.592G>C , LRG_572t1:c.592G>C
|
NP_000304.2:p.Asp198His
|
|
NM_001314077.1:c.688G>C , LRG_572t2:c.688G>C
|
NP_001301006.1:p.Asp230His
|
|
NM_000313.4:c.592G>C
MANE Select
|
NP_000304.2:p.Asp198His
|
|
NM_001314077.2:c.688G>C
|
NP_001301006.1:p.Asp230His
|
|