ENST00000650516.2:c.853+569G>T
|
ENSP00000498052.2:n.853+569G>T
|
|
ENST00000343257.7:c.827G>T
MANE Select
|
ENSP00000339867.2:p.Gly276Val
|
|
ENST00000432192.6:c.651G>T
|
|
|
ENST00000455478.6:c.415G>T
|
ENSP00000400027.2:n.415G>T
|
|
ENST00000650516.1:c.853+569G>T
|
ENSP00000498052.1:n.853+569G>T
|
|
ENST00000343257.6:c.827G>T
|
ENSP00000339867.2:p.Gly276Val
|
|
ENST00000432192.5:c.341G>T
|
|
|
ENST00000455478.5:c.419G>T
|
|
|
ENST00000495612.1:n.154+2618G>T
|
|
|
NM_000083.2:c.827G>T
|
NP_000074.2:p.Gly276Val
|
|
NR_046453.1:n.917G>T
|
|
|
XM_011515781.1:c.853+569G>T
|
XP_011514083.1:n.853+569G>T
|
|
XM_017011739.1:c.403+2618G>T
|
XP_016867228.1:n.403+2618G>T
|
|
XM_017011740.1:c.403+2618G>T
|
XP_016867229.1:n.403+2618G>T
|
|
NM_000083.3:c.827G>T
MANE Select
|
NP_000074.3:p.Gly276Val
|
|
NR_046453.2:n.932G>T
|
|
|