ENST00000372899.6:c.475G>C
|
ENSP00000361990.1:p.Glu159Gln
|
|
ENST00000372901.2:c.475G>C
MANE Select
|
ENSP00000361992.1:p.Glu159Gln
|
|
ENST00000372899.5:c.475G>C
|
ENSP00000361990.1:p.Glu159Gln
|
|
ENST00000372901.1:c.475G>C
|
ENSP00000361992.1:p.Glu159Gln
|
|
ENST00000372903.6:c.475G>C
|
ENSP00000361994.2:p.Glu159Gln
|
|
NM_001184801.1:c.475G>C
|
NP_001171730.1:p.Glu159Gln
|
|
NM_015255.2:c.475G>C
|
NP_056070.1:p.Glu159Gln
|
|
XM_005248965.3:c.475G>C
|
XP_005249022.1:p.Glu159Gln
|
|
XM_011514438.1:c.289G>C
|
XP_011512740.1:p.Glu97Gln
|
|
XM_011514442.1:c.475G>C
|
XP_011512744.1:p.Glu159Gln
|
|
NM_001363705.1:c.475G>C
|
NP_001350634.1:p.Glu159Gln
|
|
XM_005248966.3:c.-1631G>C
|
XP_005249023.1:n.-1631G>C
|
|
XM_011514438.2:c.556G>C
|
XP_011512740.2:p.Glu186Gln
|
|
XM_017010594.1:c.556G>C
|
XP_016866083.1:p.Glu186Gln
|
|
XM_017010595.1:c.556G>C
|
XP_016866084.1:p.Glu186Gln
|
|
XM_017010596.1:c.475G>C
|
XP_016866085.1:p.Glu159Gln
|
|
XM_017010597.1:c.556G>C
|
XP_016866086.1:p.Glu186Gln
|
|
XR_001743284.2:n.974G>C
|
|
|
XR_001743285.1:n.975G>C
|
|
|
NM_001184801.2:c.475G>C
|
NP_001171730.1:p.Glu159Gln
|
|
NM_001363705.2:c.475G>C
MANE Select
|
NP_001350634.1:p.Glu159Gln
|
|
NM_015255.3:c.475G>C
|
NP_056070.1:p.Glu159Gln
|
|