|
NM_032119.4:c.8488C>G
MANE Select
|
NP_115495.3:p.Leu2830Val
|
|
ENST00000405460.9:c.8488C>G
MANE Select
|
ENSP00000384582.2:p.Leu2830Val
|
|
NM_032119.3:c.8488C>G
|
NP_115495.3:p.Leu2830Val
|
|
NR_003149.1:n.8501C>G
|
|
|
NR_003149.2:n.8504C>G
|
|
|
ENST00000405460.6:c.8488C>G
|
ENSP00000384582.2:p.Leu2830Val
|
|
ENST00000509621.1:c.1185C>G
|
|
|
ENST00000639431.1:c.265+29292C>G
|
ENSP00000491057.1:n.265+29292C>G
|
|
ENST00000639473.1:n.3947C>G
|
|
|
ENST00000640012.1:c.2295C>G
|
|
|
ENST00000640374.1:n.1632C>G
|
|
|
ENST00000640403.1:c.5779C>G
|
ENSP00000492531.1:p.Leu1927Val
|
|
ENST00000640779.1:c.3217C>G
|
|
|
XM_011543675.1:c.8485C>G
|
XP_011541977.1:p.Leu2829Val
|
|
XM_011543676.1:c.8407C>G
|
XP_011541978.1:p.Leu2803Val
|
|
XM_011543677.1:c.5791C>G
|
XP_011541979.1:p.Leu1931Val
|
|
XM_011543678.1:c.8488C>G
|
XP_011541980.1:p.Leu2830Val
|
|
XM_011543679.1:c.8488C>G
|
XP_011541981.1:p.Leu2830Val
|
|
XM_017009963.2:c.8509C>G
|
XP_016865452.1:p.Leu2837Val
|
|
XM_017009964.2:c.8506C>G
|
XP_016865453.1:p.Leu2836Val
|
|
XM_017009965.1:c.8506C>G
|
XP_016865454.1:p.Leu2836Val
|
|
XM_017009966.2:c.8428C>G
|
XP_016865455.1:p.Leu2810Val
|
|
XM_017009967.1:c.8413C>G
|
XP_016865456.1:p.Leu2805Val
|
|
XM_017009968.2:c.8509C>G
|
XP_016865457.1:p.Leu2837Val
|
|
XM_017009969.2:c.8509C>G
|
XP_016865458.1:p.Leu2837Val
|
|
XM_017009970.2:c.8509C>G
|
XP_016865459.1:p.Leu2837Val
|
|
XM_017009971.2:c.8509C>G
|
XP_016865460.1:p.Leu2837Val
|
|
XM_017009972.1:c.1627C>G
|
XP_016865461.1:p.Leu543Val
|
|
XM_017009973.1:c.1606C>G
|
XP_016865462.1:p.Leu536Val
|
|
XM_017009974.2:c.8509C>G
|
XP_016865463.1:p.Leu2837Val
|