ENST00000651522.1:c.42T>C
|
ENSP00000498290.1:p.Tyr14=
|
|
ENST00000651570.2:c.333T>C
MANE Select
|
ENSP00000498421.1:p.Tyr111=
|
|
ENST00000651583.1:c.288T>C
|
ENSP00000498821.1:p.Tyr96=
|
|
ENST00000219066.5:c.357T>C
|
ENSP00000219066.1:p.Tyr119=
|
|
ENST00000561841.1:c.253T>C
|
|
|
ENST00000562120.1:n.66T>C
|
|
|
ENST00000566380.5:c.296T>C
|
|
|
ENST00000568513.5:c.173+131T>C
|
|
|
NM_002528.5:c.357T>C
|
NP_002519.1:p.Tyr119=
|
|
XM_011522505.1:c.357T>C
|
XP_011520807.1:p.Tyr119=
|
|
NM_001318193.1:c.357T>C
|
NP_001305122.1:p.Tyr119=
|
|
NM_001318194.1:c.24+131T>C
|
NP_001305123.1:n.24+131T>C
|
|
NM_002528.6:c.357T>C
|
NP_002519.1:p.Tyr119=
|
|
XM_017023253.1:c.357T>C
|
XP_016878742.1:p.Tyr119=
|
|
NM_001318193.2:c.333T>C
|
NP_001305122.2:p.Tyr111=
|
|
NM_002528.7:c.333T>C
MANE Select
|
NP_002519.2:p.Tyr111=
|
|
NM_001318194.2:c.24+131T>C
|
NP_001305123.1:n.24+131T>C
|
|