|
ENST00000367400.8:c.3172G>T
MANE Select
|
ENSP00000356370.3:p.Glu1058Ter
|
|
|
ENST00000638467.1:c.3172G>T
|
ENSP00000491102.1:p.Glu1058Ter
|
|
|
ENST00000681519.1:c.2053G>T
|
ENSP00000505267.1:p.Glu685Ter
|
|
|
ENST00000367397.1:c.1315G>T
|
ENSP00000356367.1:p.Glu439Ter
|
|
|
ENST00000367399.6:c.2836G>T
|
ENSP00000356369.2:p.Glu946Ter
|
|
|
ENST00000367400.7:c.3172G>T
|
ENSP00000356370.3:p.Glu1058Ter
|
|
|
ENST00000484075.5:c.3172G>T
|
ENSP00000433932.1:p.Glu1058Ter
|
|
|
ENST00000535699.5:c.3100G>T
|
ENSP00000438786.1:p.Glu1034Ter
|
|
|
ENST00000538660.5:c.2129-565G>T
|
ENSP00000438091.1:n.2129-565G>T
|
|
|
NM_001193640.1:c.2836G>T
|
NP_001180569.1:p.Glu946Ter
|
|
|
NM_001257965.1:c.3100G>T
|
NP_001244894.1:p.Glu1034Ter
|
|
|
NM_001257966.1:c.2129-565G>T
|
NP_001244895.1:n.2129-565G>T
|
|
|
NM_201253.2:c.3172G>T
|
NP_957705.1:p.Glu1058Ter
|
|
|
NR_047563.1:n.3173G>T
|
|
|
|
NR_047564.1:n.3381G>T
|
|
|
|
XM_011509365.1:c.3172G>T
|
XP_011507667.1:p.Glu1058Ter
|
|
|
XM_011509366.1:c.3172G>T
|
XP_011507668.1:p.Glu1058Ter
|
|
|
XM_011509367.1:c.3172G>T
|
XP_011507669.1:p.Glu1058Ter
|
|
|
XM_011509368.1:c.2590G>T
|
XP_011507670.1:p.Glu864Ter
|
|
|
XM_011509369.1:c.1615G>T
|
XP_011507671.1:p.Glu539Ter
|
|
|
XM_011509365.2:c.3172G>T
|
XP_011507667.1:p.Glu1058Ter
|
|
|
XM_011509369.2:c.1615G>T
|
XP_011507671.1:p.Glu539Ter
|
|
|
XM_017000851.1:c.2329G>T
|
XP_016856340.1:p.Glu777Ter
|
|
|
XM_017000852.1:c.3307G>T
|
XP_016856341.1:p.Glu1103Ter
|
|
|
NM_201253.3:c.3172G>T
MANE Select
|
NP_957705.1:p.Glu1058Ter
|
|
|
NM_001193640.2:c.2836G>T
|
NP_001180569.1:p.Glu946Ter
|
|
|
NM_001257965.2:c.3100G>T
|
NP_001244894.1:p.Glu1034Ter
|
|
|
NR_047563.2:n.3125G>T
|
|
|
|
NR_047564.2:n.3333G>T
|
|
|
|
NM_001257966.2:c.2129-565G>T
|
NP_001244895.1:n.2129-565G>T
|
|
