|
ENST00000356839.10:c.480C>G
MANE Select
|
ENSP00000349297.5:p.Tyr160Ter
|
|
|
ENST00000322910.9:c.*435C>G
|
ENSP00000325395.5:n.*435C>G
|
|
|
ENST00000350303.9:c.414C>G
|
ENSP00000344152.5:p.Tyr138Ter
|
|
|
ENST00000356839.9:c.480C>G
|
ENSP00000349297.5:p.Tyr160Ter
|
|
|
ENST00000543245.6:c.549C>G
|
ENSP00000438689.2:p.Tyr183Ter
|
|
|
ENST00000577191.5:n.557C>G
|
|
|
|
ENST00000577433.5:n.688C>G
|
|
|
|
ENST00000577857.5:n.296C>G
|
|
|
|
ENST00000579286.5:n.661C>G
|
|
|
|
ENST00000579886.2:c.318C>G
|
ENSP00000463246.1:p.Tyr106Ter
|
|
|
ENST00000580365.1:n.211C>G
|
|
|
|
ENST00000581378.5:c.198C>G
|
|
|
|
ENST00000581562.5:n.525-412C>G
|
|
|
|
ENST00000582166.1:n.461C>G
|
|
|
|
ENST00000583312.5:c.480C>G
|
ENSP00000467920.1:p.Tyr160Ter
|
|
|
ENST00000583760.1:n.262C>G
|
|
|
|
NM_000018.3:c.480C>G
|
NP_000009.1:p.Tyr160Ter
|
|
|
NM_001033859.2:c.414C>G
|
NP_001029031.1:p.Tyr138Ter
|
|
|
NM_001270447.1:c.549C>G
|
NP_001257376.1:p.Tyr183Ter
|
|
|
NM_001270448.1:c.252C>G
|
NP_001257377.1:p.Tyr84Ter
|
|
|
XM_006721516.2:c.480C>G
|
XP_006721579.2:p.Tyr160Ter
|
|
|
XM_011523829.1:c.480C>G
|
XP_011522131.1:p.Tyr160Ter
|
|
|
XM_011523830.1:c.480C>G
|
XP_011522132.1:p.Tyr160Ter
|
|
|
XR_934021.1:n.587C>G
|
|
|
|
XR_934022.1:n.587C>G
|
|
|
|
XR_934023.1:n.587C>G
|
|
|
|
XM_006721516.3:c.480C>G
|
XP_006721579.2:p.Tyr160Ter
|
|
|
XM_011523829.2:c.480C>G
|
XP_011522131.1:p.Tyr160Ter
|
|
|
XM_011523830.2:c.480C>G
|
XP_011522132.1:p.Tyr160Ter
|
|
|
XM_024450741.1:c.480C>G
|
XP_024306509.1:p.Tyr160Ter
|
|
|
XR_934021.2:n.539C>G
|
|
|
|
XR_934022.2:n.539C>G
|
|
|
|
XR_934023.2:n.539C>G
|
|
|
|
NM_000018.4:c.480C>G
MANE Select
|
NP_000009.1:p.Tyr160Ter
|
|
|
NM_001033859.3:c.414C>G
|
NP_001029031.1:p.Tyr138Ter
|
|
|
NM_001270447.2:c.549C>G
|
NP_001257376.1:p.Tyr183Ter
|
|
|
NM_001270448.2:c.252C>G
|
NP_001257377.1:p.Tyr84Ter
|
|
