ENST00000525346.6:c.1205T>G
|
ENSP00000435707.3:p.Val402Gly
|
|
ENST00000526780.6:c.1205T>G
|
ENSP00000435668.2:p.Val402Gly
|
|
ENST00000527316.6:c.1031T>G
|
ENSP00000435047.2:p.Val344Gly
|
|
ENST00000682708.1:c.1256T>G
|
ENSP00000506866.1:p.Val419Gly
|
|
ENST00000683287.1:c.1241T>G
|
ENSP00000507607.1:p.Val414Gly
|
|
ENST00000683714.1:c.1213T>G
|
ENSP00000508207.1:p.Trp405Gly
|
|
ENST00000684396.1:n.1245T>G
|
|
|
ENST00000685320.1:c.620T>G
|
ENSP00000509319.1:p.Val207Gly
|
|
ENST00000690257.1:c.1109T>G
|
ENSP00000510750.1:p.Val370Gly
|
|
ENST00000355527.8:c.1205T>G
MANE Select
|
ENSP00000347717.4:p.Val402Gly
|
|
ENST00000355527.7:c.1205T>G
|
ENSP00000347717.3:p.Val402Gly
|
|
ENST00000407721.6:c.1205T>G
|
ENSP00000384739.2:p.Val402Gly
|
|
ENST00000525137.1:c.706T>G
|
ENSP00000435956.1:p.Trp236Gly
|
|
ENST00000533800.5:c.455T>G
|
ENSP00000435011.1:p.Val152Gly
|
|
ENST00000534795.5:c.319+2214T>G
|
|
|
NM_001163817.1:c.1205T>G
|
NP_001157289.1:p.Val402Gly
|
|
NM_001360.2:c.1205T>G , LRG_340t1:c.1205T>G
|
NP_001351.2:p.Val402Gly
|
|
XM_011544777.1:c.1339T>G
|
XP_011543079.1:p.Trp447Gly
|
|
XM_011544777.2:c.1339T>G
|
XP_011543079.1:p.Trp447Gly
|
|
NM_001163817.2:c.1205T>G
|
NP_001157289.1:p.Val402Gly
|
|
NM_001360.3:c.1205T>G
MANE Select
|
NP_001351.2:p.Val402Gly
|
|