ENST00000405460.9:c.10216G>A
MANE Select
|
ENSP00000384582.2:p.Gly3406Ser
|
|
ENST00000639431.1:c.265+52514G>A
|
ENSP00000491057.1:n.265+52514G>A
|
|
ENST00000640374.1:n.3360G>A
|
|
|
ENST00000640464.1:n.635G>A
|
|
|
ENST00000405460.6:c.10216G>A
|
ENSP00000384582.2:p.Gly3406Ser
|
|
ENST00000509621.1:c.2913G>A
|
|
|
NM_032119.3:c.10216G>A
|
NP_115495.3:p.Gly3406Ser
|
|
NR_003149.1:n.10229G>A
|
|
|
XM_011543675.1:c.10213G>A
|
XP_011541977.1:p.Gly3405Ser
|
|
XM_011543676.1:c.10135G>A
|
XP_011541978.1:p.Gly3379Ser
|
|
XM_011543677.1:c.7519G>A
|
XP_011541979.1:p.Gly2507Ser
|
|
XM_011543678.1:c.10216G>A
|
XP_011541980.1:p.Gly3406Ser
|
|
XM_011543679.1:c.10216G>A
|
XP_011541981.1:p.Gly3406Ser
|
|
XR_948560.1:n.271+12184C>T
|
|
|
NM_032119.4:c.10216G>A
MANE Select
|
NP_115495.3:p.Gly3406Ser
|
|
XM_017009963.2:c.10237G>A
|
XP_016865452.1:p.Gly3413Ser
|
|
XM_017009964.2:c.10234G>A
|
XP_016865453.1:p.Gly3412Ser
|
|
XM_017009965.1:c.10234G>A
|
XP_016865454.1:p.Gly3412Ser
|
|
XM_017009966.2:c.10156G>A
|
XP_016865455.1:p.Gly3386Ser
|
|
XM_017009967.1:c.10141G>A
|
XP_016865456.1:p.Gly3381Ser
|
|
XM_017009968.2:c.10237G>A
|
XP_016865457.1:p.Gly3413Ser
|
|
XM_017009969.2:c.10237G>A
|
XP_016865458.1:p.Gly3413Ser
|
|
XM_017009970.2:c.10237G>A
|
XP_016865459.1:p.Gly3413Ser
|
|
XM_017009971.2:c.10237G>A
|
XP_016865460.1:p.Gly3413Ser
|
|
XM_017009972.1:c.3355G>A
|
XP_016865461.1:p.Gly1119Ser
|
|
XM_017009973.1:c.3334G>A
|
XP_016865462.1:p.Gly1112Ser
|
|
XM_017009974.2:c.10237G>A
|
XP_016865463.1:p.Gly3413Ser
|
|
XR_001742802.1:n.2522+12184C>T
|
|
|
NR_003149.2:n.10232G>A
|
|
|