ENST00000354393.7:c.2270G=
|
ENSP00000346369.2:p.Gly757=
|
|
ENST00000540630.6:c.3149G=
|
ENSP00000441668.3:p.Gly1050=
|
|
ENST00000613327.5:c.3095G=
|
ENSP00000480757.2:p.Gly1032=
|
|
ENST00000688812.1:c.*358G=
|
ENSP00000510658.1:n.*358G=
|
|
ENST00000690544.1:c.*2366G=
|
ENSP00000508989.1:n.*2366G=
|
|
ENST00000358913.10:c.3095G=
MANE Select
|
ENSP00000351790.5:p.Gly1032=
|
|
ENST00000354393.6:c.2270G=
|
ENSP00000346369.2:p.Gly757=
|
|
ENST00000358913.9:c.3095G=
|
ENSP00000351790.5:p.Gly1032=
|
|
ENST00000540630.5:c.3095G=
|
ENSP00000441668.2:p.Gly1032=
|
|
ENST00000613327.4:c.2213G=
|
ENSP00000480757.1:p.Gly738=
|
|
NM_001256267.1:c.3095G=
|
NP_001243196.1:p.Gly1032=
|
|
NM_001256268.1:c.2213G=
|
NP_001243197.1:p.Gly738=
|
|
NM_032578.3:c.3095G= , LRG_410t1:c.3095G=
|
NP_115967.2:p.Gly1032=
|
|
NR_045662.3:n.2522G=
|
|
|
NR_045663.3:n.3224G=
|
|
|
XM_006718043.2:c.3149G=
|
XP_006718106.1:p.Gly1050=
|
|
XM_011540292.1:c.3125G=
|
XP_011538594.1:p.Gly1042=
|
|
XM_017016833.1:c.3173G=
|
XP_016872322.1:p.Gly1058=
|
|
XM_017016834.2:c.3095G=
|
XP_016872323.1:p.Gly1032=
|
|
XM_024448236.1:c.1973G=
|
XP_024304004.1:p.Gly658=
|
|
NR_045662.4:n.2632G=
|
|
|
NR_045663.4:n.3169G=
|
|
|
NM_001256267.2:c.3095G=
|
NP_001243196.1:p.Gly1032=
|
|
NM_001256268.2:c.2213G=
|
NP_001243197.1:p.Gly738=
|
|
NM_032578.4:c.3095G=
MANE Select
|
NP_115967.2:p.Gly1032=
|
|