ENST00000269260.7:c.876G>C
MANE Select
|
ENSP00000269260.2:p.Gly292=
|
|
ENST00000269260.6:c.876G>C
|
ENSP00000269260.2:p.Gly292=
|
|
ENST00000346341.6:c.831G>C
|
ENSP00000341895.2:p.Gly277=
|
|
ENST00000381488.10:c.831G>C
|
ENSP00000370898.6:p.Gly277=
|
|
ENST00000412477.7:c.939G>C
|
ENSP00000403701.3:p.Gly313=
|
|
ENST00000571206.1:c.300G>C
|
ENSP00000460607.1:p.Gly100=
|
|
ENST00000571428.5:c.300G>C
|
ENSP00000465877.1:p.Gly100=
|
|
ENST00000572457.5:c.300G>C
|
ENSP00000465296.1:p.Gly100=
|
|
ENST00000574502.5:c.*354G>C
|
ENSP00000458371.1:n.*354G>C
|
|
ENST00000574954.5:c.300G>C
|
ENSP00000466344.1:p.Gly100=
|
|
ENST00000575877.5:c.786+90G>C
|
ENSP00000466857.1:n.786+90G>C
|
|
ENST00000576235.1:c.758G>C
|
ENSP00000460879.1:n.758G>C
|
|
NM_001257328.1:c.939G>C
|
NP_001244257.1:p.Gly313=
|
|
NM_001257329.1:c.786+90G>C
|
NP_001244258.1:n.786+90G>C
|
|
NM_001257330.1:c.876G>C
|
NP_001244259.1:p.Gly292=
|
|
NM_001257331.1:c.831G>C
|
NP_001244260.1:p.Gly277=
|
|
NM_004313.3:c.876G>C
|
NP_004304.1:p.Gly292=
|
|
NM_199004.1:c.831G>C
|
NP_945355.1:p.Gly277=
|
|
NR_047516.1:n.1073G>C
|
|
|
XM_006721520.1:c.300G>C
|
XP_006721583.1:p.Gly100=
|
|
XM_006721521.1:c.300G>C
|
XP_006721584.1:p.Gly100=
|
|
XM_011523858.1:c.969G>C
|
XP_011522160.1:p.Gly323=
|
|
XM_011523859.1:c.924G>C
|
XP_011522161.1:p.Gly308=
|
|
NM_001330064.1:c.300G>C
|
NP_001316993.1:p.Gly100=
|
|
XM_011523858.2:c.969G>C
|
XP_011522160.1:p.Gly323=
|
|
XM_017024645.1:c.300G>C
|
XP_016880134.1:p.Gly100=
|
|
XM_024450751.1:c.876G>C
|
XP_024306519.1:p.Gly292=
|
|
XM_024450752.1:c.300G>C
|
XP_024306520.1:p.Gly100=
|
|
XM_024450753.1:c.300G>C
|
XP_024306521.1:p.Gly100=
|
|
XR_002958006.1:n.883G>C
|
|
|
XR_002958007.1:n.883G>C
|
|
|
NM_004313.4:c.876G>C
MANE Select
|
NP_004304.1:p.Gly292=
|
|
NM_001257328.2:c.939G>C
|
NP_001244257.1:p.Gly313=
|
|
NM_001257329.2:c.786+90G>C
|
NP_001244258.1:n.786+90G>C
|
|
NM_001257330.2:c.876G>C
|
NP_001244259.1:p.Gly292=
|
|
NM_001257331.2:c.831G>C
|
NP_001244260.1:p.Gly277=
|
|
NM_001330064.2:c.300G>C
|
NP_001316993.1:p.Gly100=
|
|
NM_199004.2:c.831G>C
|
NP_945355.1:p.Gly277=
|
|
NR_047516.2:n.935G>C
|
|
|