ENST00000301030.10:c.5794G>A
MANE Select
|
ENSP00000301030.4:p.Glu1932Lys
|
|
ENST00000330736.10:c.*5597G>A
|
ENSP00000330815.5:n.*5597G>A
|
|
ENST00000378330.7:c.5794G>A
|
ENSP00000367581.2:p.Glu1932Lys
|
|
ENST00000642600.1:c.5794G>A
|
ENSP00000495226.1:p.Glu1932Lys
|
|
ENST00000644285.1:c.745-5557G>A
|
ENSP00000496476.1:n.745-5557G>A
|
|
ENST00000301030.8:c.5794G>A
|
ENSP00000301030.4:p.Glu1932Lys
|
|
ENST00000330736.9:c.*5597G>A
|
ENSP00000330815.5:n.*5597G>A
|
|
ENST00000378330.6:c.5794G>A
|
ENSP00000367581.2:p.Glu1932Lys
|
|
ENST00000562194.1:c.152-5557G>A
|
|
|
NM_001256182.1:c.5794G>A
|
NP_001243111.1:p.Glu1932Lys
|
|
NM_001256183.1:c.5794G>A
|
NP_001243112.1:p.Glu1932Lys
|
|
NM_013275.5:c.5794G>A
|
NP_037407.4:p.Glu1932Lys
|
|
XM_006721181.1:c.5692G>A
|
XP_006721244.1:p.Glu1898Lys
|
|
XM_006721184.2:c.5497G>A
|
XP_006721247.1:p.Glu1833Lys
|
|
XM_011523051.1:c.5794G>A
|
XP_011521353.1:p.Glu1932Lys
|
|
XM_011523052.1:c.5794G>A
|
XP_011521354.1:p.Glu1932Lys
|
|
XM_011523053.1:c.5794G>A
|
XP_011521355.1:p.Glu1932Lys
|
|
XM_011523054.1:c.5692G>A
|
XP_011521356.1:p.Glu1898Lys
|
|
XM_011523055.1:c.5692G>A
|
XP_011521357.1:p.Glu1898Lys
|
|
XM_011523056.1:c.5665G>A
|
XP_011521358.1:p.Glu1889Lys
|
|
XM_011523057.1:c.5794G>A
|
XP_011521359.1:p.Glu1932Lys
|
|
XM_011523051.3:c.5794G>A
|
XP_011521353.1:p.Glu1932Lys
|
|
XM_011523053.2:c.5794G>A
|
XP_011521355.1:p.Glu1932Lys
|
|
XM_011523054.2:c.5692G>A
|
XP_011521356.1:p.Glu1898Lys
|
|
XM_011523055.2:c.5692G>A
|
XP_011521357.1:p.Glu1898Lys
|
|
XM_011523056.2:c.5665G>A
|
XP_011521358.1:p.Glu1889Lys
|
|
XM_011523057.2:c.5794G>A
|
XP_011521359.1:p.Glu1932Lys
|
|
XM_017023182.2:c.5794G>A
|
XP_016878671.1:p.Glu1932Lys
|
|
XM_017023183.1:c.5794G>A
|
XP_016878672.1:p.Glu1932Lys
|
|
XM_017023184.1:c.5794G>A
|
XP_016878673.1:p.Glu1932Lys
|
|
XM_017023185.1:c.5794G>A
|
XP_016878674.1:p.Glu1932Lys
|
|
XM_017023186.1:c.5794G>A
|
XP_016878675.1:p.Glu1932Lys
|
|
XM_017023187.1:c.5794G>A
|
XP_016878676.1:p.Glu1932Lys
|
|
XM_024450244.1:c.5692G>A
|
XP_024306012.1:p.Glu1898Lys
|
|
NM_013275.6:c.5794G>A
MANE Select
|
NP_037407.4:p.Glu1932Lys
|
|
NM_001256182.2:c.5794G>A
|
NP_001243111.1:p.Glu1932Lys
|
|
NM_001256183.2:c.5794G>A
|
NP_001243112.1:p.Glu1932Lys
|
|