ENST00000405460.9:c.7069A>G
MANE Select
|
ENSP00000384582.2:p.Met2357Val
|
|
ENST00000639431.1:c.265+16513A>G
|
ENSP00000491057.1:n.265+16513A>G
|
|
ENST00000639473.1:n.2528A>G
|
|
|
ENST00000640012.1:c.876A>G
|
|
|
ENST00000640374.1:n.213A>G
|
|
|
ENST00000640403.1:c.4360A>G
|
ENSP00000492531.1:p.Met1454Val
|
|
ENST00000640779.1:c.1798A>G
|
|
|
ENST00000405460.6:c.7069A>G
|
ENSP00000384582.2:p.Met2357Val
|
|
NM_032119.3:c.7069A>G
|
NP_115495.3:p.Met2357Val
|
|
NR_003149.1:n.7082A>G
|
|
|
XM_011543675.1:c.7066A>G
|
XP_011541977.1:p.Met2356Val
|
|
XM_011543676.1:c.6988A>G
|
XP_011541978.1:p.Met2330Val
|
|
XM_011543677.1:c.4372A>G
|
XP_011541979.1:p.Met1458Val
|
|
XM_011543678.1:c.7069A>G
|
XP_011541980.1:p.Met2357Val
|
|
XM_011543679.1:c.7069A>G
|
XP_011541981.1:p.Met2357Val
|
|
NM_032119.4:c.7069A>G
MANE Select
|
NP_115495.3:p.Met2357Val
|
|
XM_017009963.2:c.7069A>G
|
XP_016865452.1:p.Met2357Val
|
|
XM_017009964.2:c.7066A>G
|
XP_016865453.1:p.Met2356Val
|
|
XM_017009965.1:c.7066A>G
|
XP_016865454.1:p.Met2356Val
|
|
XM_017009966.2:c.6988A>G
|
XP_016865455.1:p.Met2330Val
|
|
XM_017009967.1:c.6973A>G
|
XP_016865456.1:p.Met2325Val
|
|
XM_017009968.2:c.7069A>G
|
XP_016865457.1:p.Met2357Val
|
|
XM_017009969.2:c.7069A>G
|
XP_016865458.1:p.Met2357Val
|
|
XM_017009970.2:c.7069A>G
|
XP_016865459.1:p.Met2357Val
|
|
XM_017009971.2:c.7069A>G
|
XP_016865460.1:p.Met2357Val
|
|
XM_017009972.1:c.187A>G
|
XP_016865461.1:p.Met63Val
|
|
XM_017009973.1:c.187A>G
|
XP_016865462.1:p.Met63Val
|
|
XM_017009974.2:c.7069A>G
|
XP_016865463.1:p.Met2357Val
|
|
NR_003149.2:n.7085A>G
|
|
|