|
ENST00000261769.10:c.2373C>T
MANE Select
|
ENSP00000261769.4:p.Leu791=
|
|
|
ENST00000261769.9:c.2373C>T
|
ENSP00000261769.4:p.Leu791=
|
|
|
ENST00000422392.6:c.2190C>T
|
ENSP00000414946.2:p.Leu730=
|
|
|
ENST00000562118.1:n.591C>T
|
|
|
|
ENST00000562836.5:n.2444C>T
|
|
|
|
ENST00000566510.5:c.*1039C>T
|
ENSP00000458139.1:n.*1039C>T
|
|
|
ENST00000566612.5:c.*613C>T
|
ENSP00000454782.1:n.*613C>T
|
|
|
ENST00000611625.4:c.2436C>T
|
ENSP00000481063.1:p.Leu812=
|
|
|
ENST00000612417.4:c.1853+3177C>T
|
ENSP00000478360.1:n.1853+3177C>T
|
|
|
ENST00000621016.4:c.1866-4472C>T
|
ENSP00000480664.1:n.1866-4472C>T
|
|
|
NM_004360.3:c.2373C>T , LRG_301t1:c.2373C>T
|
NP_004351.1:p.Leu791=
|
|
|
XM_011523488.1:c.1638C>T
|
XP_011521790.1:p.Leu546=
|
|
|
XM_011523489.1:c.1638C>T
|
XP_011521791.1:p.Leu546=
|
|
|
NM_001317184.1:c.2190C>T
|
NP_001304113.1:p.Leu730=
|
|
|
NM_001317185.1:c.825C>T
|
NP_001304114.1:p.Leu275=
|
|
|
NM_001317186.1:c.408C>T
|
NP_001304115.1:p.Leu136=
|
|
|
NM_004360.4:c.2373C>T
|
NP_004351.1:p.Leu791=
|
|
|
NM_004360.5:c.2373C>T
MANE Select
|
NP_004351.1:p.Leu791=
|
|
|
NM_001317184.2:c.2190C>T
|
NP_001304113.1:p.Leu730=
|
|
|
NM_001317185.2:c.825C>T
|
NP_001304114.1:p.Leu275=
|
|
|
NM_001317186.2:c.408C>T
|
NP_001304115.1:p.Leu136=
|
|
