ENST00000285021.12:c.2304T>C
MANE Select
|
ENSP00000285021.8:p.Pro768=
|
|
ENST00000285021.11:c.2304T>C
|
ENSP00000285021.7:p.Pro768=
|
|
ENST00000427795.2:n.169T>C
|
|
|
ENST00000476581.6:c.*1757T>C
|
ENSP00000424548.1:n.*1757T>C
|
|
NM_004628.4:c.2304T>C , LRG_472t1:c.2304T>C
|
NP_004619.3:p.Pro768=
|
|
NR_027299.1:n.2284T>C
|
|
|
XM_011534092.1:c.2304T>C
|
XP_011532394.1:p.Pro768=
|
|
NM_001354726.1:c.1725T>C
|
NP_001341655.1:p.Pro575=
|
|
NM_001354727.1:c.2298T>C
|
NP_001341656.1:p.Pro766=
|
|
NM_001354729.1:c.2286T>C
|
NP_001341658.1:p.Pro762=
|
|
NM_001354730.1:c.2058T>C
|
NP_001341659.1:p.Pro686=
|
|
NR_148950.1:n.2247T>C
|
|
|
NR_148951.1:n.2123T>C
|
|
|
XR_001740256.2:n.2337T>C
|
|
|
XR_002959580.1:n.2337T>C
|
|
|
XR_002959581.1:n.3954T>C
|
|
|
NM_001354727.2:c.2298T>C
|
NP_001341656.1:p.Pro766=
|
|
NM_004628.5:c.2304T>C
MANE Select
|
NP_004619.3:p.Pro768=
|
|
NR_148950.2:n.2176T>C
|
|
|
NR_148951.2:n.2052T>C
|
|
|
NM_001354726.2:c.1725T>C
|
NP_001341655.1:p.Pro575=
|
|
NM_001354729.2:c.2286T>C
|
NP_001341658.1:p.Pro762=
|
|
NM_001354730.2:c.2058T>C
|
NP_001341659.1:p.Pro686=
|
|