ENST00000317357.10:c.1767G>T
MANE Select
|
ENSP00000318900.5:p.Gln589His
|
|
ENST00000317357.9:c.1767G>T
|
ENSP00000318900.5:p.Gln589His
|
|
NM_018013.3:c.1767G>T
|
NP_060483.3:p.Gln589His
|
|
XM_005267041.3:c.1920G>T
|
XP_005267098.1:p.Gln640His
|
|
XM_005267042.3:c.1824G>T
|
XP_005267099.1:p.Gln608His
|
|
XM_011535920.1:c.1920G>T
|
XP_011534222.1:p.Gln640His
|
|
XM_011535921.1:c.1806G>T
|
XP_011534223.1:p.Gln602His
|
|
XM_011535922.1:c.1179G>T
|
XP_011534224.1:p.Gln393His
|
|
XM_011535923.1:c.990G>T
|
XP_011534225.1:p.Gln330His
|
|
XM_005267041.4:c.1920G>T
|
XP_005267098.1:p.Gln640His
|
|
XM_005267042.4:c.1824G>T
|
XP_005267099.1:p.Gln608His
|
|
XM_011535920.2:c.1920G>T
|
XP_011534222.1:p.Gln640His
|
|
XM_011535921.2:c.1806G>T
|
XP_011534223.1:p.Gln602His
|
|
XM_011535923.2:c.990G>T
|
XP_011534225.1:p.Gln330His
|
|
XM_017010991.1:c.1320G>T
|
XP_016866480.1:p.Gln440His
|
|
XM_017010992.1:c.1320G>T
|
XP_016866481.1:p.Gln440His
|
|
XM_017010993.1:c.1320G>T
|
XP_016866482.1:p.Gln440His
|
|
XM_017010994.1:c.1320G>T
|
XP_016866483.1:p.Gln440His
|
|
NM_018013.4:c.1767G>T
MANE Select
|
NP_060483.3:p.Gln589His
|
|