ENST00000247933.9:c.1721G>T
|
ENSP00000247933.4:p.Gly574Val
|
|
ENST00000514224.2:c.1721G>T
MANE Select
|
ENSP00000425081.2:p.Gly574Val
|
|
ENST00000652070.1:n.1777G>T
|
|
|
ENST00000247933.8:c.1721G>T
|
ENSP00000247933.4:p.Gly574Val
|
|
ENST00000514224.1:c.1325G>T
|
ENSP00000425081.1:p.Gly442Val
|
|
ENST00000514417.1:n.113G>T
|
|
|
ENST00000514698.5:n.1828G>T
|
|
|
NM_000203.4:c.1721G>T
|
NP_000194.2:p.Gly574Val
|
|
NR_110313.1:n.1809G>T
|
|
|
XM_006713882.2:c.1325G>T
|
XP_006713945.1:p.Gly442Val
|
|
XM_011513459.1:c.1787G>T
|
XP_011511761.1:p.Gly596Val
|
|
XM_011513460.1:c.1580G>T
|
XP_011511762.1:p.Gly527Val
|
|
XM_011513461.1:c.1514G>T
|
XP_011511763.1:p.Gly505Val
|
|
XM_011513462.1:c.1433G>T
|
XP_011511764.1:p.Gly478Val
|
|
XM_011513463.1:c.1433G>T
|
XP_011511765.1:p.Gly478Val
|
|
XR_924947.1:n.1977G>T
|
|
|
NM_000203.5:c.1721G>T
MANE Select
|
NP_000194.2:p.Gly574Val
|
|
NM_001363576.1:c.1325G>T
|
NP_001350505.1:p.Gly442Val
|
|
XM_011513461.2:c.1514G>T
|
XP_011511763.1:p.Gly505Val
|
|
XM_017008163.1:c.761G>T
|
XP_016863652.1:p.Gly254Val
|
|