ENST00000359785.10:c.915+1717G>A
(PTPN22)
MANE Select
|
ENSP00000352833.5:n.915+1717G>A
|
|
ENST00000359785.9:c.915+1717G>A
(PTPN22)
|
ENSP00000352833.5:n.915+1717G>A
|
|
ENST00000420377.6:c.915+1717G>A
(PTPN22)
|
ENSP00000388229.2:n.915+1717G>A
|
|
ENST00000460620.5:c.468+9559G>A
(PTPN22)
|
ENSP00000433141.1:n.468+9559G>A
|
|
ENST00000484147.5:n.956+1717G>A
(PTPN22)
|
|
|
ENST00000525799.1:c.534+1717G>A
(PTPN22)
|
ENSP00000432674.1:n.534+1717G>A
|
|
ENST00000528414.5:c.750+7648G>A
(PTPN22)
|
ENSP00000435176.1:n.750+7648G>A
|
|
ENST00000532224.5:c.*193+1717G>A
(PTPN22)
|
ENSP00000431249.1:n.*193+1717G>A
|
|
ENST00000538253.5:c.843+1717G>A
(PTPN22)
|
ENSP00000439372.2:n.843+1717G>A
|
|
NM_001193431.1:c.915+1717G>A
(PTPN22)
|
NP_001180360.1:n.915+1717G>A
|
|
NM_001193431.2:c.915+1717G>A
(PTPN22)
|
NP_001180360.1:n.915+1717G>A
|
|
NM_001308297.1:c.843+1717G>A
(PTPN22)
|
NP_001295226.1:n.843+1717G>A
|
|
NM_012411.4:c.750+7648G>A
(PTPN22)
|
NP_036543.4:n.750+7648G>A
|
|
NM_012411.5:c.750+7648G>A
(PTPN22)
|
NP_036543.4:n.750+7648G>A
|
|
NM_015967.5:c.915+1717G>A
(PTPN22)
|
NP_057051.3:n.915+1717G>A
|
|
NM_015967.6:c.915+1717G>A
(PTPN22)
|
NP_057051.3:n.915+1717G>A
|
|
NR_125965.1:n.414+31351C>T
(AP4B1-AS1)
|
|
|
XM_011541221.1:c.837+1717G>A
(PTPN22)
|
XP_011539523.1:n.837+1717G>A
|
|
XM_011541222.1:c.915+1717G>A
(PTPN22)
|
XP_011539524.1:n.915+1717G>A
|
|
XM_011541223.1:c.915+1717G>A
(PTPN22)
|
XP_011539525.1:n.915+1717G>A
|
|
XM_011541224.1:c.471+1717G>A
(PTPN22)
|
XP_011539526.1:n.471+1717G>A
|
|
XM_011541225.1:c.843+1717G>A
(PTPN22)
|
XP_011539527.1:n.843+1717G>A
|
|
XM_011541223.2:c.915+1717G>A
(PTPN22)
|
XP_011539525.1:n.915+1717G>A
|
|
XM_011541225.2:c.843+1717G>A
(PTPN22)
|
XP_011539527.1:n.843+1717G>A
|
|
XM_017001004.1:c.915+1717G>A
(PTPN22)
|
XP_016856493.1:n.915+1717G>A
|
|
XM_017001005.2:c.570+1717G>A
(PTPN22)
|
XP_016856494.1:n.570+1717G>A
|
|
XM_017001006.1:c.915+1717G>A
(PTPN22)
|
XP_016856495.1:n.915+1717G>A
|
|
NM_015967.7:c.915+1717G>A
(PTPN22)
|
NP_057051.3:n.915+1717G>A
|
|
NM_015967.8:c.915+1717G>A
(PTPN22)
MANE Select
|
NP_057051.4:n.915+1717G>A
|
|