ENST00000260818.11:c.2564A>C
MANE Select
|
ENSP00000260818.6:p.Asn855Thr
|
|
ENST00000650455.1:c.*712A>C
|
ENSP00000496825.1:n.*712A>C
|
|
ENST00000260818.10:c.2564A>C
|
ENSP00000260818.6:p.Asn855Thr
|
|
ENST00000464766.1:n.401A>C
|
|
|
NM_015268.3:c.2564A>C
|
NP_056083.3:p.Asn855Thr
|
|
XM_005247245.3:c.2579A>C
|
XP_005247302.1:p.Asn860Thr
|
|
NM_001329126.1:c.2579A>C
|
NP_001316055.1:p.Asn860Thr
|
|
XM_017006036.1:c.533A>C
|
XP_016861525.1:p.Asn178Thr
|
|
NM_015268.4:c.2564A>C
MANE Select
|
NP_056083.3:p.Asn855Thr
|
|
NM_001329126.2:c.2579A>C
|
NP_001316055.1:p.Asn860Thr
|
|