ENST00000261769.10:c.2005C>G
MANE Select
|
ENSP00000261769.4:p.Leu669Val
|
|
ENST00000261769.9:c.2005C>G
|
ENSP00000261769.4:p.Leu669Val
|
|
ENST00000422392.6:c.1822C>G
|
ENSP00000414946.2:p.Leu608Val
|
|
ENST00000562118.1:n.223C>G
|
|
|
ENST00000562836.5:n.2076C>G
|
|
|
ENST00000566510.5:c.*671C>G
|
ENSP00000458139.1:n.*671C>G
|
|
ENST00000566612.5:c.*245C>G
|
ENSP00000454782.1:n.*245C>G
|
|
ENST00000611625.4:c.2068C>G
|
ENSP00000481063.1:p.Leu690Val
|
|
ENST00000612417.4:c.1830+1348C>G
|
ENSP00000478360.1:n.1830+1348C>G
|
|
ENST00000621016.4:c.1865+1313C>G
|
ENSP00000480664.1:n.1865+1313C>G
|
|
NM_004360.3:c.2005C>G , LRG_301t1:c.2005C>G
|
NP_004351.1:p.Leu669Val
|
|
XM_011523488.1:c.1270C>G
|
XP_011521790.1:p.Leu424Val
|
|
XM_011523489.1:c.1270C>G
|
XP_011521791.1:p.Leu424Val
|
|
NM_001317184.1:c.1822C>G
|
NP_001304113.1:p.Leu608Val
|
|
NM_001317185.1:c.457C>G
|
NP_001304114.1:p.Leu153Val
|
|
NM_001317186.1:c.40C>G
|
NP_001304115.1:p.Leu14Val
|
|
NM_004360.4:c.2005C>G
|
NP_004351.1:p.Leu669Val
|
|
NM_004360.5:c.2005C>G
MANE Select
|
NP_004351.1:p.Leu669Val
|
|
NM_001317184.2:c.1822C>G
|
NP_001304113.1:p.Leu608Val
|
|
NM_001317185.2:c.457C>G
|
NP_001304114.1:p.Leu153Val
|
|
NM_001317186.2:c.40C>G
|
NP_001304115.1:p.Leu14Val
|
|