ENST00000374840.8:c.897G>A
MANE Select
|
ENSP00000363973.3:p.Leu299=
|
|
ENST00000374830.2:c.73-2034G>A
|
|
|
ENST00000374832.5:c.897G>A
|
ENSP00000363965.1:p.Leu299=
|
|
ENST00000374840.7:c.897G>A
|
ENSP00000363973.3:p.Leu299=
|
|
ENST00000539907.5:c.666G>A
|
ENSP00000437674.1:p.Leu222=
|
|
ENST00000540617.5:c.732G>A
|
ENSP00000442672.1:p.Leu244=
|
|
NM_000478.4:c.897G>A
|
NP_000469.3:p.Leu299=
|
|
NM_001127501.2:c.732G>A
|
NP_001120973.2:p.Leu244=
|
|
NM_001177520.1:c.666G>A
|
NP_001170991.1:p.Leu222=
|
|
XM_005245818.1:c.897G>A
|
XP_005245875.1:p.Leu299=
|
|
XM_005245820.2:c.897G>A
|
XP_005245877.1:p.Leu299=
|
|
XM_006710546.1:c.897G>A
|
XP_006710609.1:p.Leu299=
|
|
NM_000478.5:c.897G>A
|
NP_000469.3:p.Leu299=
|
|
NM_001127501.3:c.732G>A
|
NP_001120973.2:p.Leu244=
|
|
NM_001177520.2:c.666G>A
|
NP_001170991.1:p.Leu222=
|
|
XM_006710546.3:c.897G>A
|
XP_006710609.1:p.Leu299=
|
|
XM_017000903.1:c.741G>A
|
XP_016856392.1:p.Leu247=
|
|
NM_000478.6:c.897G>A
MANE Select
|
NP_000469.3:p.Leu299=
|
|
NM_001127501.4:c.732G>A
|
NP_001120973.2:p.Leu244=
|
|
NM_001177520.3:c.666G>A
|
NP_001170991.1:p.Leu222=
|
|
NM_001369803.2:c.897G>A
|
NP_001356732.1:p.Leu299=
|
|
NM_001369804.2:c.897G>A
|
NP_001356733.1:p.Leu299=
|
|
NM_001369805.2:c.897G>A
|
NP_001356734.1:p.Leu299=
|
|