ENST00000651522.1:c.34C>T
|
ENSP00000498290.1:p.His12Tyr
|
|
ENST00000651570.2:c.325C>T
MANE Select
|
ENSP00000498421.1:p.His109Tyr
|
|
ENST00000651583.1:c.280C>T
|
ENSP00000498821.1:p.His94Tyr
|
|
ENST00000219066.5:c.349C>T
|
ENSP00000219066.1:p.His117Tyr
|
|
ENST00000561841.1:c.245C>T
|
|
|
ENST00000562120.1:n.58C>T
|
|
|
ENST00000566380.5:c.288C>T
|
|
|
ENST00000568513.5:c.173+123C>T
|
|
|
NM_002528.5:c.349C>T
|
NP_002519.1:p.His117Tyr
|
|
XM_011522505.1:c.349C>T
|
XP_011520807.1:p.His117Tyr
|
|
NM_001318193.1:c.349C>T
|
NP_001305122.1:p.His117Tyr
|
|
NM_001318194.1:c.24+123C>T
|
NP_001305123.1:n.24+123C>T
|
|
NM_002528.6:c.349C>T
|
NP_002519.1:p.His117Tyr
|
|
XM_017023253.1:c.349C>T
|
XP_016878742.1:p.His117Tyr
|
|
NM_001318193.2:c.325C>T
|
NP_001305122.2:p.His109Tyr
|
|
NM_002528.7:c.325C>T
MANE Select
|
NP_002519.2:p.His109Tyr
|
|
NM_001318194.2:c.24+123C>T
|
NP_001305123.1:n.24+123C>T
|
|