ENST00000356839.10:c.435A>T
MANE Select
|
ENSP00000349297.5:p.Gln145His
|
|
ENST00000322910.9:c.*390A>T
|
ENSP00000325395.5:n.*390A>T
|
|
ENST00000350303.9:c.369A>T
|
ENSP00000344152.5:p.Gln123His
|
|
ENST00000356839.9:c.435A>T
|
ENSP00000349297.5:p.Gln145His
|
|
ENST00000543245.6:c.504A>T
|
ENSP00000438689.2:p.Gln168His
|
|
ENST00000577191.5:n.512A>T
|
|
|
ENST00000577433.5:n.643A>T
|
|
|
ENST00000577857.5:n.293+186A>T
|
|
|
ENST00000579286.5:n.616A>T
|
|
|
ENST00000579886.2:c.273A>T
|
ENSP00000463246.1:p.Gln91His
|
|
ENST00000580365.1:n.166A>T
|
|
|
ENST00000581378.5:c.134A>T
|
|
|
ENST00000581562.5:n.482A>T
|
|
|
ENST00000582056.5:n.618A>T
|
|
|
ENST00000582166.1:n.416A>T
|
|
|
ENST00000583312.5:c.435A>T
|
ENSP00000467920.1:p.Gln145His
|
|
ENST00000584103.5:c.468A>T
|
ENSP00000465353.1:p.Gln156His
|
|
NM_000018.3:c.435A>T
|
NP_000009.1:p.Gln145His
|
|
NM_001033859.2:c.369A>T
|
NP_001029031.1:p.Gln123His
|
|
NM_001270447.1:c.504A>T
|
NP_001257376.1:p.Gln168His
|
|
NM_001270448.1:c.207A>T
|
NP_001257377.1:p.Gln69His
|
|
XM_006721516.2:c.435A>T
|
XP_006721579.2:p.Gln145His
|
|
XM_011523829.1:c.435A>T
|
XP_011522131.1:p.Gln145His
|
|
XM_011523830.1:c.435A>T
|
XP_011522132.1:p.Gln145His
|
|
XR_934021.1:n.542A>T
|
|
|
XR_934022.1:n.542A>T
|
|
|
XR_934023.1:n.542A>T
|
|
|
XM_006721516.3:c.435A>T
|
XP_006721579.2:p.Gln145His
|
|
XM_011523829.2:c.435A>T
|
XP_011522131.1:p.Gln145His
|
|
XM_011523830.2:c.435A>T
|
XP_011522132.1:p.Gln145His
|
|
XM_024450741.1:c.435A>T
|
XP_024306509.1:p.Gln145His
|
|
XR_934021.2:n.494A>T
|
|
|
XR_934022.2:n.494A>T
|
|
|
XR_934023.2:n.494A>T
|
|
|
NM_000018.4:c.435A>T
MANE Select
|
NP_000009.1:p.Gln145His
|
|
NM_001033859.3:c.369A>T
|
NP_001029031.1:p.Gln123His
|
|
NM_001270447.2:c.504A>T
|
NP_001257376.1:p.Gln168His
|
|
NM_001270448.2:c.207A>T
|
NP_001257377.1:p.Gln69His
|
|