ENST00000405460.9:c.851T>G
MANE Select
|
ENSP00000384582.2:p.Val284Gly
|
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ENST00000640083.1:n.556T>G
|
|
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ENST00000640109.1:n.947T>G
|
|
|
ENST00000640281.1:n.910T>G
|
|
|
ENST00000405460.6:c.851T>G
|
ENSP00000384582.2:p.Val284Gly
|
|
NM_032119.3:c.851T>G
|
NP_115495.3:p.Val284Gly
|
|
NR_003149.1:n.947T>G
|
|
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XM_011543675.1:c.851T>G
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XP_011541977.1:p.Val284Gly
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|
XM_011543676.1:c.851T>G
|
XP_011541978.1:p.Val284Gly
|
|
XM_011543678.1:c.851T>G
|
XP_011541980.1:p.Val284Gly
|
|
XM_011543679.1:c.851T>G
|
XP_011541981.1:p.Val284Gly
|
|
NM_032119.4:c.851T>G
MANE Select
|
NP_115495.3:p.Val284Gly
|
|
XM_017009963.2:c.851T>G
|
XP_016865452.1:p.Val284Gly
|
|
XM_017009964.2:c.851T>G
|
XP_016865453.1:p.Val284Gly
|
|
XM_017009965.1:c.848T>G
|
XP_016865454.1:p.Val283Gly
|
|
XM_017009966.2:c.851T>G
|
XP_016865455.1:p.Val284Gly
|
|
XM_017009967.1:c.755T>G
|
XP_016865456.1:p.Val252Gly
|
|
XM_017009968.2:c.851T>G
|
XP_016865457.1:p.Val284Gly
|
|
XM_017009969.2:c.851T>G
|
XP_016865458.1:p.Val284Gly
|
|
XM_017009970.2:c.851T>G
|
XP_016865459.1:p.Val284Gly
|
|
XM_017009971.2:c.851T>G
|
XP_016865460.1:p.Val284Gly
|
|
XM_017009974.2:c.851T>G
|
XP_016865463.1:p.Val284Gly
|
|
NR_003149.2:n.950T>G
|
|
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