ENST00000394867.9:n.1198G>T
|
|
|
ENST00000687128.1:n.1198G>T
|
|
|
ENST00000688002.1:n.1053G>T
|
|
|
ENST00000689792.1:n.663G>T
|
|
|
ENST00000262948.10:c.759G>T
MANE Select
|
ENSP00000262948.4:p.Met253Ile
|
|
ENST00000262948.9:c.759G>T
|
ENSP00000262948.3:p.Met253Ile
|
|
ENST00000394867.8:c.468G>T
|
ENSP00000378336.1:p.Met156Ile
|
|
ENST00000593364.5:n.706G>T
|
|
|
ENST00000595715.1:n.574G>T
|
|
|
ENST00000597263.5:n.169+1658G>T
|
|
|
ENST00000599021.1:c.29+1658G>T
|
|
|
ENST00000600584.5:n.1319G>T
|
|
|
ENST00000601786.5:n.1060G>T
|
|
|
NM_030662.3:c.759G>T , LRG_750t1:c.759G>T
|
NP_109587.1:p.Met253Ile
|
|
XM_006722799.2:c.705+1658G>T
|
XP_006722862.1:n.705+1658G>T
|
|
XM_011528133.1:c.189G>T
|
XP_011526435.1:p.Met63Ile
|
|
XM_017026989.1:c.759G>T
|
XP_016882478.1:p.Met253Ile
|
|
XM_017026990.1:c.705+1658G>T
|
XP_016882479.1:n.705+1658G>T
|
|
NM_030662.4:c.759G>T
MANE Select
|
NP_109587.1:p.Met253Ile
|
|