ENST00000255266.10:c.1700T>G
MANE Select
|
ENSP00000255266.5:p.Val567Gly
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ENST00000255266.9:c.1700T>G
|
ENSP00000255266.5:p.Val567Gly
|
|
ENST00000508173.5:n.1884T>G
|
|
|
ENST00000613228.1:c.1457T>G
|
ENSP00000478060.1:p.Val486Gly
|
|
ENST00000617647.4:c.1457T>G
|
ENSP00000482774.1:p.Val486Gly
|
|
NM_000440.2:c.1700T>G
|
NP_000431.2:p.Val567Gly
|
|
XM_011537648.1:c.1700T>G
|
XP_011535950.1:p.Val567Gly
|
|
XM_011537649.1:c.1154T>G
|
XP_011535951.1:p.Val385Gly
|
|
XM_011537650.1:c.815T>G
|
XP_011535952.1:p.Val272Gly
|
|
XM_011537651.1:c.653T>G
|
XP_011535953.1:p.Val218Gly
|
|
XM_011537652.1:c.623T>G
|
XP_011535954.1:p.Val208Gly
|
|
XM_011537653.1:c.623T>G
|
XP_011535955.1:p.Val208Gly
|
|
XM_011537654.1:c.623T>G
|
XP_011535956.1:p.Val208Gly
|
|
XM_011537650.2:c.815T>G
|
XP_011535952.1:p.Val272Gly
|
|
XM_011537651.2:c.653T>G
|
XP_011535953.1:p.Val218Gly
|
|
XM_011537653.2:c.623T>G
|
XP_011535955.1:p.Val208Gly
|
|
XM_011537654.2:c.623T>G
|
XP_011535956.1:p.Val208Gly
|
|
XM_017009572.2:c.1457T>G
|
XP_016865061.1:p.Val486Gly
|
|
NM_000440.3:c.1700T>G
MANE Select
|
NP_000431.2:p.Val567Gly
|
|