ENST00000354393.7:c.2252G=
|
ENSP00000346369.2:p.Gly751=
|
|
ENST00000540630.6:c.3131G=
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ENSP00000441668.3:p.Gly1044=
|
|
ENST00000613327.5:c.3077G=
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ENSP00000480757.2:p.Gly1026=
|
|
ENST00000688812.1:c.*340G=
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ENSP00000510658.1:n.*340G=
|
|
ENST00000690544.1:c.*2348G=
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ENSP00000508989.1:n.*2348G=
|
|
ENST00000358913.10:c.3077G=
MANE Select
|
ENSP00000351790.5:p.Gly1026=
|
|
ENST00000354393.6:c.2252G=
|
ENSP00000346369.2:p.Gly751=
|
|
ENST00000358913.9:c.3077G=
|
ENSP00000351790.5:p.Gly1026=
|
|
ENST00000540630.5:c.3077G=
|
ENSP00000441668.2:p.Gly1026=
|
|
ENST00000613327.4:c.2195G=
|
ENSP00000480757.1:p.Gly732=
|
|
NM_001256267.1:c.3077G=
|
NP_001243196.1:p.Gly1026=
|
|
NM_001256268.1:c.2195G=
|
NP_001243197.1:p.Gly732=
|
|
NM_032578.3:c.3077G= , LRG_410t1:c.3077G=
|
NP_115967.2:p.Gly1026=
|
|
NR_045662.3:n.2504G=
|
|
|
NR_045663.3:n.3206G=
|
|
|
XM_006718043.2:c.3131G=
|
XP_006718106.1:p.Gly1044=
|
|
XM_011540292.1:c.3107G=
|
XP_011538594.1:p.Gly1036=
|
|
XM_017016833.1:c.3155G=
|
XP_016872322.1:p.Gly1052=
|
|
XM_017016834.2:c.3077G=
|
XP_016872323.1:p.Gly1026=
|
|
XM_024448236.1:c.1955G=
|
XP_024304004.1:p.Gly652=
|
|
NR_045662.4:n.2614G=
|
|
|
NR_045663.4:n.3151G=
|
|
|
NM_001256267.2:c.3077G=
|
NP_001243196.1:p.Gly1026=
|
|
NM_001256268.2:c.2195G=
|
NP_001243197.1:p.Gly732=
|
|
NM_032578.4:c.3077G=
MANE Select
|
NP_115967.2:p.Gly1026=
|
|