ENST00000405460.9:c.16271T>G
MANE Select
|
ENSP00000384582.2:p.Val5424Gly
|
|
ENST00000425867.3:c.5225T>G
|
ENSP00000392618.3:p.Val1742Gly
|
|
ENST00000638510.1:n.3538T>G
|
|
|
ENST00000639431.1:c.265+147290T>G
|
ENSP00000491057.1:n.265+147290T>G
|
|
ENST00000640061.1:n.128+1317T>G
|
|
|
ENST00000640407.1:c.2681T>G
|
ENSP00000491425.1:p.Val894Gly
|
|
ENST00000405460.6:c.16271T>G
|
ENSP00000384582.2:p.Val5424Gly
|
|
ENST00000425867.2:c.3254T>G
|
ENSP00000392618.2:p.Val1085Gly
|
|
NM_032119.3:c.16271T>G
|
NP_115495.3:p.Val5424Gly
|
|
NR_003149.1:n.16284T>G
|
|
|
XM_011543675.1:c.16268T>G
|
XP_011541977.1:p.Val5423Gly
|
|
XM_011543676.1:c.16190T>G
|
XP_011541978.1:p.Val5397Gly
|
|
XM_011543677.1:c.13574T>G
|
XP_011541979.1:p.Val4525Gly
|
|
NM_032119.4:c.16271T>G
MANE Select
|
NP_115495.3:p.Val5424Gly
|
|
XM_017009963.2:c.16292T>G
|
XP_016865452.1:p.Val5431Gly
|
|
XM_017009964.2:c.16289T>G
|
XP_016865453.1:p.Val5430Gly
|
|
XM_017009965.1:c.16289T>G
|
XP_016865454.1:p.Val5430Gly
|
|
XM_017009966.2:c.16211T>G
|
XP_016865455.1:p.Val5404Gly
|
|
XM_017009967.1:c.16196T>G
|
XP_016865456.1:p.Val5399Gly
|
|
XM_017009968.2:c.16112T>G
|
XP_016865457.1:p.Val5371Gly
|
|
XM_017009969.2:c.16292T>G
|
XP_016865458.1:p.Val5431Gly
|
|
XM_017009972.1:c.9410T>G
|
XP_016865461.1:p.Val3137Gly
|
|
XM_017009973.1:c.9389T>G
|
XP_016865462.1:p.Val3130Gly
|
|
NR_003149.2:n.16287T>G
|
|
|