ENST00000651522.1:c.21T>G
|
ENSP00000498290.1:p.His7Gln
|
|
ENST00000651570.2:c.312T>G
MANE Select
|
ENSP00000498421.1:p.His104Gln
|
|
ENST00000651583.1:c.267T>G
|
ENSP00000498821.1:p.His89Gln
|
|
ENST00000219066.5:c.336T>G
|
ENSP00000219066.1:p.His112Gln
|
|
ENST00000561841.1:c.232T>G
|
|
|
ENST00000562120.1:n.45T>G
|
|
|
ENST00000566380.5:c.275T>G
|
|
|
ENST00000568513.5:c.173+110T>G
|
|
|
NM_002528.5:c.336T>G
|
NP_002519.1:p.His112Gln
|
|
XM_011522505.1:c.336T>G
|
XP_011520807.1:p.His112Gln
|
|
NM_001318193.1:c.336T>G
|
NP_001305122.1:p.His112Gln
|
|
NM_001318194.1:c.24+110T>G
|
NP_001305123.1:n.24+110T>G
|
|
NM_002528.6:c.336T>G
|
NP_002519.1:p.His112Gln
|
|
XM_017023253.1:c.336T>G
|
XP_016878742.1:p.His112Gln
|
|
NM_001318193.2:c.312T>G
|
NP_001305122.2:p.His104Gln
|
|
NM_002528.7:c.312T>G
MANE Select
|
NP_002519.2:p.His104Gln
|
|
NM_001318194.2:c.24+110T>G
|
NP_001305123.1:n.24+110T>G
|
|