|
ENST00000647165.2:c.6414T>C
MANE Select
|
ENSP00000495481.1:p.Asn2138=
|
|
|
ENST00000205890.9:c.6414T>C
|
ENSP00000205890.5:p.Asn2138=
|
|
|
ENST00000615845.4:c.6414T>C
|
ENSP00000481642.1:p.Asn2138=
|
|
|
NM_016239.3:c.6414T>C
|
NP_057323.3:p.Asn2138=
|
|
|
XM_011523917.1:c.6354T>C
|
XP_011522219.1:p.Asn2118=
|
|
|
XM_011523918.1:c.6342+12T>C
|
XP_011522220.1:n.6342+12T>C
|
|
|
XM_011523921.1:c.6408T>C
|
XP_011522223.1:p.Asn2136=
|
|
|
XR_934037.1:n.7013T>C
|
|
|
|
XR_934038.1:n.7013T>C
|
|
|
|
XM_011523918.2:c.6342+12T>C
|
XP_011522220.1:n.6342+12T>C
|
|
|
XM_017024714.2:c.6354T>C
|
XP_016880203.1:p.Asn2118=
|
|
|
XM_017024715.2:c.6417T>C
|
XP_016880204.1:p.Asn2139=
|
|
|
XM_024450781.1:c.6213+1420T>C
|
XP_024306549.1:n.6213+1420T>C
|
|
|
NM_016239.4:c.6414T>C
MANE Select
|
NP_057323.3:p.Asn2138=
|
|
