ENST00000573725.2:c.6561C=
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ENSP00000460849.2:p.Asn2187=
|
|
ENST00000703537.1:c.2489C=
|
|
|
ENST00000703538.1:c.*6464C=
|
ENSP00000515361.1:n.*6464C=
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|
ENST00000703539.1:n.3055C=
|
|
|
ENST00000703540.1:c.6594C=
|
ENSP00000515362.1:p.Asn2198=
|
|
ENST00000703541.1:c.6606C=
|
ENSP00000515363.1:p.Asn2202=
|
|
ENST00000304992.11:c.6741C=
MANE Select
|
ENSP00000304350.6:p.Asn2247=
|
|
ENST00000304992.10:c.6741C=
|
ENSP00000304350.6:p.Asn2247=
|
|
ENST00000571958.1:c.50C=
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|
|
ENST00000572621.5:c.6741C=
|
ENSP00000460348.1:p.Asn2247=
|
|
ENST00000572723.1:n.730C=
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|
|
NM_006445.3:c.6741C=
|
NP_006436.3:p.Asn2247=
|
|
XM_024450537.1:c.6741C=
|
XP_024306305.1:p.Asn2247=
|
|
NM_006445.4:c.6741C=
MANE Select
|
NP_006436.3:p.Asn2247=
|
|