ENST00000525346.6:c.1191G>C
|
ENSP00000435707.3:p.Ser397=
|
|
ENST00000526780.6:c.1191G>C
|
ENSP00000435668.2:p.Ser397=
|
|
ENST00000527316.6:c.1017G>C
|
ENSP00000435047.2:p.Ser339=
|
|
ENST00000682708.1:c.1242G>C
|
ENSP00000506866.1:p.Ser414=
|
|
ENST00000683287.1:c.1227G>C
|
ENSP00000507607.1:p.Ser409=
|
|
ENST00000683714.1:c.1199G>C
|
ENSP00000508207.1:p.Arg400Pro
|
|
ENST00000684396.1:n.1231G>C
|
|
|
ENST00000685320.1:c.606G>C
|
ENSP00000509319.1:p.Ser202=
|
|
ENST00000690257.1:c.1095G>C
|
ENSP00000510750.1:p.Ser365=
|
|
ENST00000355527.8:c.1191G>C
MANE Select
|
ENSP00000347717.4:p.Ser397=
|
|
ENST00000355527.7:c.1191G>C
|
ENSP00000347717.3:p.Ser397=
|
|
ENST00000407721.6:c.1191G>C
|
ENSP00000384739.2:p.Ser397=
|
|
ENST00000525137.1:c.692G>C
|
ENSP00000435956.1:p.Arg231Pro
|
|
ENST00000533800.5:c.441G>C
|
ENSP00000435011.1:p.Ser147=
|
|
ENST00000534795.5:c.319+2200G>C
|
|
|
NM_001163817.1:c.1191G>C
|
NP_001157289.1:p.Ser397=
|
|
NM_001360.2:c.1191G>C , LRG_340t1:c.1191G>C
|
NP_001351.2:p.Ser397=
|
|
XM_011544777.1:c.1325G>C
|
XP_011543079.1:p.Arg442Pro
|
|
XM_011544777.2:c.1325G>C
|
XP_011543079.1:p.Arg442Pro
|
|
NM_001163817.2:c.1191G>C
|
NP_001157289.1:p.Ser397=
|
|
NM_001360.3:c.1191G>C
MANE Select
|
NP_001351.2:p.Ser397=
|
|