|
ENST00000356839.10:c.512A>G
MANE Select
|
ENSP00000349297.5:p.Asp171Gly
|
|
|
ENST00000322910.9:c.*467A>G
|
ENSP00000325395.5:n.*467A>G
|
|
|
ENST00000350303.9:c.446A>G
|
ENSP00000344152.5:p.Asp149Gly
|
|
|
ENST00000356839.9:c.512A>G
|
ENSP00000349297.5:p.Asp171Gly
|
|
|
ENST00000543245.6:c.581A>G
|
ENSP00000438689.2:p.Asp194Gly
|
|
|
ENST00000577191.5:n.589A>G
|
|
|
|
ENST00000577433.5:n.720A>G
|
|
|
|
ENST00000577857.5:n.328A>G
|
|
|
|
ENST00000579286.5:n.693A>G
|
|
|
|
ENST00000579886.2:c.350A>G
|
ENSP00000463246.1:p.Asp117Gly
|
|
|
ENST00000580365.1:n.243A>G
|
|
|
|
ENST00000581378.5:c.230A>G
|
|
|
|
ENST00000581562.5:n.525-380A>G
|
|
|
|
ENST00000582166.1:n.493A>G
|
|
|
|
ENST00000583312.5:c.512A>G
|
ENSP00000467920.1:p.Asp171Gly
|
|
|
ENST00000583760.1:n.294A>G
|
|
|
|
NM_000018.3:c.512A>G
|
NP_000009.1:p.Asp171Gly
|
|
|
NM_001033859.2:c.446A>G
|
NP_001029031.1:p.Asp149Gly
|
|
|
NM_001270447.1:c.581A>G
|
NP_001257376.1:p.Asp194Gly
|
|
|
NM_001270448.1:c.284A>G
|
NP_001257377.1:p.Asp95Gly
|
|
|
XM_006721516.2:c.512A>G
|
XP_006721579.2:p.Asp171Gly
|
|
|
XM_011523829.1:c.512A>G
|
XP_011522131.1:p.Asp171Gly
|
|
|
XM_011523830.1:c.512A>G
|
XP_011522132.1:p.Asp171Gly
|
|
|
XR_934021.1:n.619A>G
|
|
|
|
XR_934022.1:n.619A>G
|
|
|
|
XR_934023.1:n.619A>G
|
|
|
|
XM_006721516.3:c.512A>G
|
XP_006721579.2:p.Asp171Gly
|
|
|
XM_011523829.2:c.512A>G
|
XP_011522131.1:p.Asp171Gly
|
|
|
XM_011523830.2:c.512A>G
|
XP_011522132.1:p.Asp171Gly
|
|
|
XM_024450741.1:c.512A>G
|
XP_024306509.1:p.Asp171Gly
|
|
|
XR_934021.2:n.571A>G
|
|
|
|
XR_934022.2:n.571A>G
|
|
|
|
XR_934023.2:n.571A>G
|
|
|
|
NM_000018.4:c.512A>G
MANE Select
|
NP_000009.1:p.Asp171Gly
|
|
|
NM_001033859.3:c.446A>G
|
NP_001029031.1:p.Asp149Gly
|
|
|
NM_001270447.2:c.581A>G
|
NP_001257376.1:p.Asp194Gly
|
|
|
NM_001270448.2:c.284A>G
|
NP_001257377.1:p.Asp95Gly
|
|
