|
ENST00000261769.10:c.2362G>T
MANE Select
|
ENSP00000261769.4:p.Ala788Ser
|
|
|
ENST00000261769.9:c.2362G>T
|
ENSP00000261769.4:p.Ala788Ser
|
|
|
ENST00000422392.6:c.2179G>T
|
ENSP00000414946.2:p.Ala727Ser
|
|
|
ENST00000562118.1:n.580G>T
|
|
|
|
ENST00000562836.5:n.2433G>T
|
|
|
|
ENST00000566510.5:c.*1028G>T
|
ENSP00000458139.1:n.*1028G>T
|
|
|
ENST00000566612.5:c.*602G>T
|
ENSP00000454782.1:n.*602G>T
|
|
|
ENST00000611625.4:c.2425G>T
|
ENSP00000481063.1:p.Ala809Ser
|
|
|
ENST00000612417.4:c.1853+3166G>T
|
ENSP00000478360.1:n.1853+3166G>T
|
|
|
ENST00000621016.4:c.1866-4483G>T
|
ENSP00000480664.1:n.1866-4483G>T
|
|
|
NM_004360.3:c.2362G>T , LRG_301t1:c.2362G>T
|
NP_004351.1:p.Ala788Ser
|
|
|
XM_011523488.1:c.1627G>T
|
XP_011521790.1:p.Ala543Ser
|
|
|
XM_011523489.1:c.1627G>T
|
XP_011521791.1:p.Ala543Ser
|
|
|
NM_001317184.1:c.2179G>T
|
NP_001304113.1:p.Ala727Ser
|
|
|
NM_001317185.1:c.814G>T
|
NP_001304114.1:p.Ala272Ser
|
|
|
NM_001317186.1:c.397G>T
|
NP_001304115.1:p.Ala133Ser
|
|
|
NM_004360.4:c.2362G>T
|
NP_004351.1:p.Ala788Ser
|
|
|
NM_004360.5:c.2362G>T
MANE Select
|
NP_004351.1:p.Ala788Ser
|
|
|
NM_001317184.2:c.2179G>T
|
NP_001304113.1:p.Ala727Ser
|
|
|
NM_001317185.2:c.814G>T
|
NP_001304114.1:p.Ala272Ser
|
|
|
NM_001317186.2:c.397G>T
|
NP_001304115.1:p.Ala133Ser
|
|
