|
ENST00000531904.7:c.7531G>C
|
ENSP00000432391.3:p.Gly2511Arg
|
|
|
ENST00000710560.1:c.7522G>C
|
ENSP00000518343.1:p.Gly2508Arg
|
|
|
ENST00000649878.2:c.1471G>C
|
ENSP00000497891.2:p.Gly491Arg
|
|
|
ENST00000685397.1:c.1471G>C
|
ENSP00000509586.1:p.Gly491Arg
|
|
|
ENST00000686370.1:c.1471G>C
|
ENSP00000509179.1:p.Gly491Arg
|
|
|
ENST00000689424.1:c.1729G>C
|
ENSP00000509852.1:p.Gly577Arg
|
|
|
ENST00000691053.1:c.7504G>C
|
ENSP00000509168.1:p.Gly2502Arg
|
|
|
ENST00000389506.10:c.7423G>C
|
ENSP00000374157.5:p.Gly2475Arg
|
|
|
ENST00000528278.2:n.6774G>C
|
|
|
|
ENST00000534358.8:c.7432G>C
MANE Select
|
ENSP00000436786.2:p.Gly2478Arg
|
|
|
ENST00000649699.1:c.7309G>C
|
ENSP00000496927.1:p.Gly2437Arg
|
|
|
ENST00000389506.9:c.7423G>C
|
ENSP00000374157.5:p.Gly2475Arg
|
|
|
ENST00000528278.1:n.1559G>C
|
|
|
|
ENST00000534358.5:c.7432G>C
|
ENSP00000436786.1:p.Gly2478Arg
|
|
|
NM_001197104.1:c.7432G>C , LRG_613t1:c.7432G>C
|
NP_001184033.1:p.Gly2478Arg
|
|
|
NM_005933.3:c.7423G>C
|
NP_005924.2:p.Gly2475Arg
|
|
|
XM_006718839.2:c.4915G>C
|
XP_006718902.2:p.Gly1639Arg
|
|
|
XM_011542829.1:c.7531G>C
|
XP_011541131.1:p.Gly2511Arg
|
|
|
XM_011542830.1:c.7528G>C
|
XP_011541132.1:p.Gly2510Arg
|
|
|
XM_011542831.1:c.7522G>C
|
XP_011541133.1:p.Gly2508Arg
|
|
|
XM_011542832.1:c.5338G>C
|
XP_011541134.1:p.Gly1780Arg
|
|
|
XM_011542833.1:c.5014G>C
|
XP_011541135.1:p.Gly1672Arg
|
|
|
XM_006718839.3:c.4915G>C
|
XP_006718902.2:p.Gly1639Arg
|
|
|
XM_011542829.2:c.7531G>C
|
XP_011541131.1:p.Gly2511Arg
|
|
|
XM_011542830.2:c.7528G>C
|
XP_011541132.1:p.Gly2510Arg
|
|
|
XM_011542831.2:c.7522G>C
|
XP_011541133.1:p.Gly2508Arg
|
|
|
XM_011542833.2:c.5014G>C
|
XP_011541135.1:p.Gly1672Arg
|
|
|
NM_001197104.2:c.7432G>C
MANE Select
|
NP_001184033.1:p.Gly2478Arg
|
|
|
NM_005933.4:c.7423G>C
|
NP_005924.2:p.Gly2475Arg
|
|
