ENST00000260197.12:c.3744T>G
MANE Select
|
ENSP00000260197.6:p.Thr1248=
|
|
ENST00000260197.11:c.3744T>G
|
ENSP00000260197.6:p.Thr1248=
|
|
ENST00000525532.5:c.576T>G
|
ENSP00000434634.1:p.Thr192=
|
|
ENST00000532694.5:c.282T>G
|
ENSP00000432131.1:p.Thr94=
|
|
ENST00000534286.5:c.474T>G
|
ENSP00000436447.1:p.Thr158=
|
|
NM_003105.5:c.3744T>G
|
NP_003096.1:p.Thr1248=
|
|
XM_011542963.1:c.3630T>G
|
XP_011541265.1:p.Thr1210=
|
|
XM_011542964.1:c.3744T>G
|
XP_011541266.1:p.Thr1248=
|
|
XM_011542965.1:c.2205T>G
|
XP_011541267.1:p.Thr735=
|
|
XM_011542966.1:c.1104T>G
|
XP_011541268.1:p.Thr368=
|
|
XM_011542967.1:c.576T>G
|
XP_011541269.1:p.Thr192=
|
|
XM_011542963.3:c.3630T>G
|
XP_011541265.1:p.Thr1210=
|
|
XM_011542965.3:c.2205T>G
|
XP_011541267.1:p.Thr735=
|
|
XM_011542967.3:c.576T>G
|
XP_011541269.1:p.Thr192=
|
|
XM_017018169.2:c.3432T>G
|
XP_016873658.1:p.Thr1144=
|
|
XM_017018170.2:c.3219T>G
|
XP_016873659.1:p.Thr1073=
|
|
XM_017018171.1:c.3744T>G
|
XP_016873660.1:p.Thr1248=
|
|
XM_017018172.2:c.1104T>G
|
XP_016873661.1:p.Thr368=
|
|
NM_003105.6:c.3744T>G
MANE Select
|
NP_003096.2:p.Thr1248=
|
|