ENST00000294304.12:c.1799T>G
MANE Select
|
ENSP00000294304.6:p.Val600Gly
|
|
ENST00000294304.11:c.1799T>G
|
ENSP00000294304.6:p.Val600Gly
|
|
ENST00000529993.5:c.*211T>G
|
ENSP00000436652.1:n.*211T>G
|
|
NM_001291902.1:c.-139T>G
|
NP_001278831.1:n.-139T>G
|
|
NM_002335.3:c.1799T>G
|
NP_002326.2:p.Val600Gly
|
|
XM_005273994.2:c.1799T>G
|
XP_005274051.1:p.Val600Gly
|
|
XM_011545029.1:c.1826T>G
|
XP_011543331.1:p.Val609Gly
|
|
XM_011545030.1:c.1826T>G
|
XP_011543332.1:p.Val609Gly
|
|
XM_011545031.1:c.1826T>G
|
XP_011543333.1:p.Val609Gly
|
|
XR_949925.1:n.1841T>G
|
|
|
XR_949926.1:n.1841T>G
|
|
|
XR_001747874.1:n.1841T>G
|
|
|
XR_949925.2:n.1841T>G
|
|
|
XR_949926.2:n.1841T>G
|
|
|
NM_002335.4:c.1799T>G
MANE Select
|
NP_002326.2:p.Val600Gly
|
|
NM_001291902.2:c.-139T>G
|
NP_001278831.1:n.-139T>G
|
|