ENST00000317357.10:c.1987C>T
MANE Select
|
ENSP00000318900.5:p.Arg663Trp
|
|
ENST00000317357.9:c.1987C>T
|
ENSP00000318900.5:p.Arg663Trp
|
|
NM_018013.3:c.1987C>T
|
NP_060483.3:p.Arg663Trp
|
|
XM_005267041.3:c.2140C>T
|
XP_005267098.1:p.Arg714Trp
|
|
XM_005267042.3:c.2044C>T
|
XP_005267099.1:p.Arg682Trp
|
|
XM_011535920.1:c.2140C>T
|
XP_011534222.1:p.Arg714Trp
|
|
XM_011535921.1:c.2026C>T
|
XP_011534223.1:p.Arg676Trp
|
|
XM_011535922.1:c.1399C>T
|
XP_011534224.1:p.Arg467Trp
|
|
XM_011535923.1:c.1210C>T
|
XP_011534225.1:p.Arg404Trp
|
|
XM_005267041.4:c.2140C>T
|
XP_005267098.1:p.Arg714Trp
|
|
XM_005267042.4:c.2044C>T
|
XP_005267099.1:p.Arg682Trp
|
|
XM_011535920.2:c.2140C>T
|
XP_011534222.1:p.Arg714Trp
|
|
XM_011535921.2:c.2026C>T
|
XP_011534223.1:p.Arg676Trp
|
|
XM_011535923.2:c.1210C>T
|
XP_011534225.1:p.Arg404Trp
|
|
XM_017010991.1:c.1540C>T
|
XP_016866480.1:p.Arg514Trp
|
|
XM_017010992.1:c.1540C>T
|
XP_016866481.1:p.Arg514Trp
|
|
XM_017010993.1:c.1540C>T
|
XP_016866482.1:p.Arg514Trp
|
|
XM_017010994.1:c.1540C>T
|
XP_016866483.1:p.Arg514Trp
|
|
NM_018013.4:c.1987C>T
MANE Select
|
NP_060483.3:p.Arg663Trp
|
|