ENST00000356839.10:c.998C>T
MANE Select
|
ENSP00000349297.5:p.Ala333Val
|
|
ENST00000322910.9:c.*953C>T
|
ENSP00000325395.5:n.*953C>T
|
|
ENST00000350303.9:c.932C>T
|
ENSP00000344152.5:p.Ala311Val
|
|
ENST00000356839.9:c.998C>T
|
ENSP00000349297.5:p.Ala333Val
|
|
ENST00000543245.6:c.1067C>T
|
ENSP00000438689.2:p.Ala356Val
|
|
ENST00000578824.5:n.147C>T
|
|
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ENST00000581378.5:c.716C>T
|
|
|
ENST00000582379.1:n.382C>T
|
|
|
ENST00000583858.5:c.27C>T
|
|
|
NM_000018.3:c.998C>T
|
NP_000009.1:p.Ala333Val
|
|
NM_001033859.2:c.932C>T
|
NP_001029031.1:p.Ala311Val
|
|
NM_001270447.1:c.1067C>T
|
NP_001257376.1:p.Ala356Val
|
|
NM_001270448.1:c.770C>T
|
NP_001257377.1:p.Ala257Val
|
|
XM_006721516.2:c.998C>T
|
XP_006721579.2:p.Ala333Val
|
|
XM_011523829.1:c.998C>T
|
XP_011522131.1:p.Ala333Val
|
|
XM_011523830.1:c.998C>T
|
XP_011522132.1:p.Ala333Val
|
|
XR_934021.1:n.1105C>T
|
|
|
XR_934022.1:n.1105C>T
|
|
|
XR_934023.1:n.1105C>T
|
|
|
XM_006721516.3:c.998C>T
|
XP_006721579.2:p.Ala333Val
|
|
XM_011523829.2:c.998C>T
|
XP_011522131.1:p.Ala333Val
|
|
XM_011523830.2:c.998C>T
|
XP_011522132.1:p.Ala333Val
|
|
XM_024450741.1:c.998C>T
|
XP_024306509.1:p.Ala333Val
|
|
XR_934021.2:n.1057C>T
|
|
|
XR_934022.2:n.1057C>T
|
|
|
XR_934023.2:n.1057C>T
|
|
|
NM_000018.4:c.998C>T
MANE Select
|
NP_000009.1:p.Ala333Val
|
|
NM_001033859.3:c.932C>T
|
NP_001029031.1:p.Ala311Val
|
|
NM_001270447.2:c.1067C>T
|
NP_001257376.1:p.Ala356Val
|
|
NM_001270448.2:c.770C>T
|
NP_001257377.1:p.Ala257Val
|
|