ENST00000262367.10:c.4395-213G>C
MANE Select
|
ENSP00000262367.5:n.4395-213G>C
|
|
ENST00000262367.9:c.4395-213G>C
|
ENSP00000262367.5:n.4395-213G>C
|
|
ENST00000382070.7:c.4281-213G>C
|
ENSP00000371502.3:n.4281-213G>C
|
|
ENST00000570939.2:c.3030-213G>C
|
ENSP00000461002.2:n.3030-213G>C
|
|
ENST00000574740.1:n.216-213G>C
|
|
|
ENST00000576720.1:n.3218-213G>C
|
|
|
NM_001079846.1:c.4281-213G>C
|
NP_001073315.1:n.4281-213G>C
|
|
NM_004380.2:c.4395-213G>C
|
NP_004371.2:n.4395-213G>C
|
|
XM_005255124.3:c.4350-213G>C
|
XP_005255181.1:n.4350-213G>C
|
|
XM_005255125.3:c.3978-213G>C
|
XP_005255182.1:n.3978-213G>C
|
|
XM_006720848.2:c.4134-213G>C
|
XP_006720911.1:n.4134-213G>C
|
|
XM_011522380.1:c.4341-213G>C
|
XP_011520682.1:n.4341-213G>C
|
|
XM_011522381.1:c.3642-213G>C
|
XP_011520683.1:n.3642-213G>C
|
|
XM_005255124.4:c.4350-213G>C
|
XP_005255181.1:n.4350-213G>C
|
|
XM_005255125.4:c.3978-213G>C
|
XP_005255182.1:n.3978-213G>C
|
|
XM_006720848.3:c.4134-213G>C
|
XP_006720911.1:n.4134-213G>C
|
|
XM_011522381.2:c.3642-213G>C
|
XP_011520683.1:n.3642-213G>C
|
|
XM_017022944.1:c.4389-213G>C
|
XP_016878433.1:n.4389-213G>C
|
|
NM_004380.3:c.4395-213G>C
MANE Select
|
NP_004371.2:n.4395-213G>C
|
|