ENST00000323798.8:c.1325_1326delinsCT
MANE Select
|
ENSP00000317904.3:p.Pro442=
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|
ENST00000263276.6:c.1133_1134delinsCT
|
ENSP00000263276.6:p.Pro378=
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|
ENST00000323798.7:c.1325_1326delinsCT
|
ENSP00000317904.3:p.Pro442=
|
|
ENST00000472004.5:n.80_81delinsCT
|
|
|
ENST00000496048.1:n.232_233delinsCT
|
|
|
NM_001161587.1:c.1133_1134delinsCT
|
NP_001155059.1:p.Pro378=
|
|
NM_002103.4:c.1325_1326delinsCT
|
NP_002094.2:p.Pro442=
|
|
NR_027763.1:n.1384_1385delinsCT
|
|
|
NM_002103.5:c.1325_1326delinsCT
MANE Select
|
NP_002094.2:p.Pro442=
|
|
NM_001161587.2:c.1133_1134delinsCT
|
NP_001155059.1:p.Pro378=
|
|
NR_027763.2:n.1340_1341delinsCT
|
|
|