|
NM_030662.4:c.844C>T
MANE Select
|
NP_109587.1:p.Pro282Ser
|
|
ENST00000262948.10:c.844C>T
MANE Select
|
ENSP00000262948.4:p.Pro282Ser
|
|
NM_030662.3:c.844C>T , LRG_750t1:c.844C>T
|
NP_109587.1:p.Pro282Ser
|
|
ENST00000262948.9:c.844C>T
|
ENSP00000262948.3:p.Pro282Ser
|
|
ENST00000394867.8:c.553C>T
|
ENSP00000378336.1:p.Pro185Ser
|
|
ENST00000394867.9:n.1283C>T
|
|
|
ENST00000593364.5:n.791C>T
|
|
|
ENST00000595715.1:n.659C>T
|
|
|
ENST00000597263.5:n.169+1743C>T
|
|
|
ENST00000599021.1:c.29+1743C>T
|
|
|
ENST00000600584.5:n.1404C>T
|
|
|
ENST00000601786.5:n.1145C>T
|
|
|
ENST00000687128.1:n.1283C>T
|
|
|
ENST00000688002.1:n.1138C>T
|
|
|
ENST00000689792.1:n.748C>T
|
|
|
XM_006722799.2:c.705+1743C>T
|
XP_006722862.1:n.705+1743C>T
|
|
XM_011528133.1:c.274C>T
|
XP_011526435.1:p.Pro92Ser
|
|
XM_017026989.1:c.844C>T
|
XP_016882478.1:p.Pro282Ser
|
|
XM_017026990.1:c.705+1743C>T
|
XP_016882479.1:n.705+1743C>T
|
