|
ENST00000261769.10:c.733C>A
MANE Select
|
ENSP00000261769.4:p.Pro245Thr
|
|
|
ENST00000261769.9:c.733C>A
|
ENSP00000261769.4:p.Pro245Thr
|
|
|
ENST00000422392.6:c.733C>A
|
ENSP00000414946.2:p.Pro245Thr
|
|
|
ENST00000561751.1:c.454+1394C>A
|
|
|
|
ENST00000562836.5:n.804C>A
|
|
|
|
ENST00000566510.5:c.577C>A
|
ENSP00000458139.1:p.Pro193Thr
|
|
|
ENST00000566612.5:c.733C>A
|
ENSP00000454782.1:p.Pro245Thr
|
|
|
ENST00000611625.4:c.733C>A
|
ENSP00000481063.1:p.Pro245Thr
|
|
|
ENST00000612417.4:c.733C>A
|
ENSP00000478360.1:p.Pro245Thr
|
|
|
ENST00000621016.4:c.733C>A
|
ENSP00000480664.1:p.Pro245Thr
|
|
|
NM_004360.3:c.733C>A , LRG_301t1:c.733C>A
|
NP_004351.1:p.Pro245Thr
|
|
|
XM_011523488.1:c.-3C>A
|
XP_011521790.1:n.-3C>A
|
|
|
XM_011523489.1:c.-3C>A
|
XP_011521791.1:n.-3C>A
|
|
|
NM_001317184.1:c.733C>A
|
NP_001304113.1:p.Pro245Thr
|
|
|
NM_001317185.1:c.-883C>A
|
NP_001304114.1:n.-883C>A
|
|
|
NM_001317186.1:c.-1087C>A
|
NP_001304115.1:n.-1087C>A
|
|
|
NM_004360.4:c.733C>A
|
NP_004351.1:p.Pro245Thr
|
|
|
NM_004360.5:c.733C>A
MANE Select
|
NP_004351.1:p.Pro245Thr
|
|
|
NM_001317184.2:c.733C>A
|
NP_001304113.1:p.Pro245Thr
|
|
|
NM_001317185.2:c.-883C>A
|
NP_001304114.1:n.-883C>A
|
|
|
NM_001317186.2:c.-1087C>A
|
NP_001304115.1:n.-1087C>A
|
|
