ENST00000474370.2:n.2432G>T
|
|
|
ENST00000492391.2:n.1583G>T
|
|
|
ENST00000682645.1:n.3530G>T
|
|
|
ENST00000683432.1:c.*634G>T
|
ENSP00000508174.1:n.*634G>T
|
|
ENST00000684207.1:c.459G>T
|
ENSP00000506942.1:p.Lys153Asn
|
|
ENST00000297157.8:c.459G>T
MANE Select
|
ENSP00000297157.3:p.Lys153Asn
|
|
ENST00000297157.7:c.459G>T
|
ENSP00000297157.3:p.Lys153Asn
|
|
ENST00000448915.1:c.357G>T
|
ENSP00000411577.1:p.Lys119Asn
|
|
NM_203288.1:c.459G>T
|
NP_976033.1:p.Lys153Asn
|
|
XM_011515468.1:c.357G>T
|
XP_011513770.1:p.Lys119Asn
|
|
XM_011515468.3:c.357G>T
|
XP_011513770.1:p.Lys119Asn
|
|
NM_203288.2:c.459G>T
MANE Select
|
NP_976033.1:p.Lys153Asn
|
|