ENST00000298910.12:c.7128G>T
MANE Select
|
ENSP00000298910.7:p.Trp2376Cys
|
|
ENST00000636518.1:c.925G>T
|
|
|
ENST00000679360.1:c.*6037G>T
|
ENSP00000505368.1:n.*6037G>T
|
|
ENST00000679532.1:c.2902G>T
|
|
|
ENST00000679683.1:c.918G>T
|
|
|
ENST00000680018.1:c.2573G>T
|
ENSP00000505347.1:n.2573G>T
|
|
ENST00000680422.1:c.4215G>T
|
|
|
ENST00000680425.1:c.2295G>T
|
ENSP00000506459.1:n.2295G>T
|
|
ENST00000680453.1:c.2585G>T
|
|
|
ENST00000680790.1:c.6873G>T
|
ENSP00000505335.1:p.Trp2291Cys
|
|
ENST00000681136.1:n.3112G>T
|
|
|
ENST00000681696.1:c.2811G>T
|
ENSP00000505871.1:p.Trp937Cys
|
|
ENST00000681773.1:n.335G>T
|
|
|
ENST00000298910.11:c.7128G>T
|
ENSP00000298910.7:p.Trp2376Cys
|
|
ENST00000430804.5:c.4424G>T
|
|
|
ENST00000479187.5:n.3809G>T
|
|
|
NM_198578.3:c.7128G>T
|
NP_940980.3:p.Trp2376Cys
|
|
XM_005268629.2:c.7128G>T
|
XP_005268686.1:p.Trp2376Cys
|
|
XM_011537877.1:c.7128G>T
|
XP_011536179.1:p.Trp2376Cys
|
|
XM_011537879.1:c.5925G>T
|
XP_011536181.1:p.Trp1975Cys
|
|
XR_944868.1:n.485-8674C>A
|
|
|
XM_005268629.4:c.7128G>T
|
XP_005268686.1:p.Trp2376Cys
|
|
XM_011537877.3:c.7128G>T
|
XP_011536179.1:p.Trp2376Cys
|
|
XM_017018787.1:c.4044G>T
|
XP_016874276.1:p.Trp1348Cys
|
|
XM_017018788.2:c.3390G>T
|
XP_016874277.1:p.Trp1130Cys
|
|
XM_024448833.1:c.5925G>T
|
XP_024304601.1:p.Trp1975Cys
|
|
XR_944868.2:n.485-8674C>A
|
|
|
NM_198578.4:c.7128G>T
MANE Select
|
NP_940980.4:p.Trp2376Cys
|
|