ENST00000448890.2:c.910G>T
|
ENSP00000409607.2:p.Glu304Ter
|
|
ENST00000461149.2:n.2127G>T
|
|
|
ENST00000696700.1:n.2162G>T
|
|
|
ENST00000696701.1:n.1014G>T
|
|
|
ENST00000696702.1:c.*386G>T
|
ENSP00000512821.1:n.*386G>T
|
|
ENST00000696703.1:c.*386G>T
|
ENSP00000512822.1:n.*386G>T
|
|
ENST00000696706.1:n.973G>T
|
|
|
ENST00000696707.1:n.1127G>T
|
|
|
ENST00000696708.1:c.*255G>T
|
ENSP00000512825.1:n.*255G>T
|
|
ENST00000696709.1:n.1312G>T
|
|
|
ENST00000696710.1:c.910G>T
|
ENSP00000512826.1:p.Glu304Ter
|
|
ENST00000696711.1:n.2359G>T
|
|
|
ENST00000696712.1:n.1026G>T
|
|
|
ENST00000696713.1:c.910G>T
|
ENSP00000512827.1:p.Glu304Ter
|
|
ENST00000696714.1:n.1386G>T
|
|
|
ENST00000696715.1:c.910G>T
|
ENSP00000512828.1:p.Glu304Ter
|
|
ENST00000378643.8:c.910G>T
MANE Select
|
ENSP00000367910.4:p.Glu304Ter
|
|
ENST00000378643.7:c.910G>T
|
ENSP00000367910.3:p.Glu304Ter
|
|
ENST00000425676.5:c.*386G>T
|
ENSP00000412793.1:n.*386G>T
|
|
ENST00000474894.1:n.115G>T
|
|
|
NM_004629.1:c.910G>T , LRG_499t1:c.910G>T
|
NP_004620.1:p.Glu304Ter
|
|
NM_004629.2:c.910G>T
MANE Select
|
NP_004620.1:p.Glu304Ter
|
|