ENST00000272895.12:c.4972G>T
MANE Select
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ENSP00000272895.7:p.Glu1658Ter
|
|
ENST00000272895.11:c.4972G>T
|
ENSP00000272895.7:p.Glu1658Ter
|
|
ENST00000389661.4:c.4018G>T
|
ENSP00000374312.4:p.Glu1340Ter
|
|
NM_015657.3:c.4018G>T
|
NP_056472.2:p.Glu1340Ter
|
|
NM_173076.2:c.4972G>T
|
NP_775099.2:p.Glu1658Ter
|
|
NR_103740.1:n.5272G>T
|
|
|
XM_011510951.1:c.4981G>T
|
XP_011509253.1:p.Glu1661Ter
|
|
XM_011510952.1:c.4981G>T
|
XP_011509254.1:p.Glu1661Ter
|
|
XM_011510951.2:c.4981G>T
|
XP_011509253.1:p.Glu1661Ter
|
|
NM_173076.3:c.4972G>T
MANE Select
|
NP_775099.2:p.Glu1658Ter
|
|
NR_103740.2:n.5470G>T
|
|
|
NM_015657.4:c.4018G>T
|
NP_056472.2:p.Glu1340Ter
|
|