ENST00000573725.2:c.6475A>G
|
ENSP00000460849.2:p.Thr2159Ala
|
|
ENST00000703537.1:c.2403A>G
|
|
|
ENST00000703538.1:c.*6378A>G
|
ENSP00000515361.1:n.*6378A>G
|
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ENST00000703539.1:n.2969A>G
|
|
|
ENST00000703540.1:c.6508A>G
|
ENSP00000515362.1:p.Thr2170Ala
|
|
ENST00000703541.1:c.6520A>G
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ENSP00000515363.1:p.Thr2174Ala
|
|
ENST00000304992.11:c.6655A>G
MANE Select
|
ENSP00000304350.6:p.Thr2219Ala
|
|
ENST00000304992.10:c.6655A>G
|
ENSP00000304350.6:p.Thr2219Ala
|
|
ENST00000572621.5:c.6655A>G
|
ENSP00000460348.1:p.Thr2219Ala
|
|
ENST00000572723.1:n.644A>G
|
|
|
NM_006445.3:c.6655A>G
|
NP_006436.3:p.Thr2219Ala
|
|
XM_024450537.1:c.6655A>G
|
XP_024306305.1:p.Thr2219Ala
|
|
NM_006445.4:c.6655A>G
MANE Select
|
NP_006436.3:p.Thr2219Ala
|
|