|
ENST00000374840.8:c.997+277_997+282dup
MANE Select
|
ENSP00000363973.3:n.997+277_997+282dup
|
|
|
ENST00000374830.2:c.73-1657_73-1652dup
|
|
|
|
ENST00000374832.5:c.997+277_997+282dup
|
ENSP00000363965.1:n.997+277_997+282dup
|
|
|
ENST00000374840.7:c.997+277_997+282dup
|
ENSP00000363973.3:n.997+277_997+282dup
|
|
|
ENST00000539907.5:c.766+277_766+282dup
|
ENSP00000437674.1:n.766+277_766+282dup
|
|
|
ENST00000540617.5:c.832+277_832+282dup
|
ENSP00000442672.1:n.832+277_832+282dup
|
|
|
NM_000478.4:c.997+277_997+282dup
|
NP_000469.3:n.997+277_997+282dup
|
|
|
NM_001127501.2:c.832+277_832+282dup
|
NP_001120973.2:n.832+277_832+282dup
|
|
|
NM_001177520.1:c.766+277_766+282dup
|
NP_001170991.1:n.766+277_766+282dup
|
|
|
XM_005245818.1:c.997+277_997+282dup
|
XP_005245875.1:n.997+277_997+282dup
|
|
|
XM_005245820.2:c.1032_1037dup
|
XP_005245877.1:p.Pro346_Gly347insGlyPro
|
|
|
XM_006710546.1:c.997+277_997+282dup
|
XP_006710609.1:n.997+277_997+282dup
|
|
|
NM_000478.5:c.997+277_997+282dup
|
NP_000469.3:n.997+277_997+282dup
|
|
|
NM_001127501.3:c.832+277_832+282dup
|
NP_001120973.2:n.832+277_832+282dup
|
|
|
NM_001177520.2:c.766+277_766+282dup
|
NP_001170991.1:n.766+277_766+282dup
|
|
|
XM_006710546.3:c.997+277_997+282dup
|
XP_006710609.1:n.997+277_997+282dup
|
|
|
XM_017000903.1:c.841+277_841+282dup
|
XP_016856392.1:n.841+277_841+282dup
|
|
|
NM_000478.6:c.997+277_997+282dup
MANE Select
|
NP_000469.3:n.997+277_997+282dup
|
|
|
NM_001127501.4:c.832+277_832+282dup
|
NP_001120973.2:n.832+277_832+282dup
|
|
|
NM_001177520.3:c.766+277_766+282dup
|
NP_001170991.1:n.766+277_766+282dup
|
|
|
NM_001369803.2:c.997+277_997+282dup
|
NP_001356732.1:n.997+277_997+282dup
|
|
|
NM_001369804.2:c.997+277_997+282dup
|
NP_001356733.1:n.997+277_997+282dup
|
|
|
NM_001369805.2:c.997+277_997+282dup
|
NP_001356734.1:n.997+277_997+282dup
|
|
