ENST00000469834.2:n.580G>C
|
|
|
ENST00000493114.2:c.492G>C
|
ENSP00000436094.2:p.Gln164His
|
|
ENST00000696871.1:c.492G>C
|
ENSP00000512940.1:p.Gln164His
|
|
ENST00000696872.1:c.552G>C
|
ENSP00000512941.1:p.Gln184His
|
|
ENST00000696873.1:c.57G>C
|
ENSP00000512942.1:p.Gln19His
|
|
ENST00000380956.9:c.492G>C
MANE Select
|
ENSP00000370343.4:p.Gln164His
|
|
ENST00000380956.8:c.492G>C
|
ENSP00000370343.4:p.Gln164His
|
|
ENST00000468485.5:n.334G>C
|
|
|
ENST00000493114.1:c.492G>C
|
ENSP00000436094.1:p.Gln164His
|
|
ENST00000495137.5:n.318G>C
|
|
|
NM_001195286.1:c.492G>C
|
NP_001182215.1:p.Gln164His
|
|
NM_002460.3:c.492G>C
|
NP_002451.2:p.Gln164His
|
|
NR_046000.2:n.618G>C
|
|
|
XM_006715090.1:c.492G>C
|
XP_006715153.1:p.Gln164His
|
|
XM_006715090.2:c.492G>C
|
XP_006715153.1:p.Gln164His
|
|
NM_002460.4:c.492G>C
MANE Select
|
NP_002451.2:p.Gln164His
|
|
NM_001195286.2:c.492G>C
|
NP_001182215.1:p.Gln164His
|
|
NR_046000.3:n.605G>C
|
|
|