|
ENST00000261769.10:c.747G>T
MANE Select
|
ENSP00000261769.4:p.Leu249Phe
|
|
|
ENST00000261769.9:c.747G>T
|
ENSP00000261769.4:p.Leu249Phe
|
|
|
ENST00000422392.6:c.747G>T
|
ENSP00000414946.2:p.Leu249Phe
|
|
|
ENST00000561751.1:c.454+1408G>T
|
|
|
|
ENST00000562836.5:n.818G>T
|
|
|
|
ENST00000566510.5:c.591G>T
|
ENSP00000458139.1:p.Leu197Phe
|
|
|
ENST00000566612.5:c.747G>T
|
ENSP00000454782.1:p.Leu249Phe
|
|
|
ENST00000611625.4:c.747G>T
|
ENSP00000481063.1:p.Leu249Phe
|
|
|
ENST00000612417.4:c.747G>T
|
ENSP00000478360.1:p.Leu249Phe
|
|
|
ENST00000621016.4:c.747G>T
|
ENSP00000480664.1:p.Leu249Phe
|
|
|
NM_004360.3:c.747G>T , LRG_301t1:c.747G>T
|
NP_004351.1:p.Leu249Phe
|
|
|
XM_011523488.1:c.12G>T
|
XP_011521790.1:p.Leu4Phe
|
|
|
XM_011523489.1:c.12G>T
|
XP_011521791.1:p.Leu4Phe
|
|
|
NM_001317184.1:c.747G>T
|
NP_001304113.1:p.Leu249Phe
|
|
|
NM_001317185.1:c.-869G>T
|
NP_001304114.1:n.-869G>T
|
|
|
NM_001317186.1:c.-1073G>T
|
NP_001304115.1:n.-1073G>T
|
|
|
NM_004360.4:c.747G>T
|
NP_004351.1:p.Leu249Phe
|
|
|
NM_004360.5:c.747G>T
MANE Select
|
NP_004351.1:p.Leu249Phe
|
|
|
NM_001317184.2:c.747G>T
|
NP_001304113.1:p.Leu249Phe
|
|
|
NM_001317185.2:c.-869G>T
|
NP_001304114.1:n.-869G>T
|
|
|
NM_001317186.2:c.-1073G>T
|
NP_001304115.1:n.-1073G>T
|
|
