|
ENST00000261769.10:c.2527G>T
MANE Select
|
ENSP00000261769.4:p.Ala843Ser
|
|
|
ENST00000261769.9:c.2527G>T
|
ENSP00000261769.4:p.Ala843Ser
|
|
|
ENST00000422392.6:c.2344G>T
|
ENSP00000414946.2:p.Ala782Ser
|
|
|
ENST00000562118.1:n.745G>T
|
|
|
|
ENST00000562836.5:n.2598G>T
|
|
|
|
ENST00000566510.5:c.*1193G>T
|
ENSP00000458139.1:n.*1193G>T
|
|
|
ENST00000566612.5:c.*767G>T
|
ENSP00000454782.1:n.*767G>T
|
|
|
ENST00000611625.4:c.2590G>T
|
ENSP00000481063.1:p.Ala864Ser
|
|
|
ENST00000612417.4:c.1854-814G>T
|
ENSP00000478360.1:n.1854-814G>T
|
|
|
ENST00000621016.4:c.1866-826G>T
|
ENSP00000480664.1:n.1866-826G>T
|
|
|
NM_004360.3:c.2527G>T , LRG_301t1:c.2527G>T
|
NP_004351.1:p.Ala843Ser
|
|
|
XM_011523488.1:c.1792G>T
|
XP_011521790.1:p.Ala598Ser
|
|
|
XM_011523489.1:c.1792G>T
|
XP_011521791.1:p.Ala598Ser
|
|
|
NM_001317184.1:c.2344G>T
|
NP_001304113.1:p.Ala782Ser
|
|
|
NM_001317185.1:c.979G>T
|
NP_001304114.1:p.Ala327Ser
|
|
|
NM_001317186.1:c.562G>T
|
NP_001304115.1:p.Ala188Ser
|
|
|
NM_004360.4:c.2527G>T
|
NP_004351.1:p.Ala843Ser
|
|
|
NM_004360.5:c.2527G>T
MANE Select
|
NP_004351.1:p.Ala843Ser
|
|
|
NM_001317184.2:c.2344G>T
|
NP_001304113.1:p.Ala782Ser
|
|
|
NM_001317185.2:c.979G>T
|
NP_001304114.1:p.Ala327Ser
|
|
|
NM_001317186.2:c.562G>T
|
NP_001304115.1:p.Ala188Ser
|
|
