|
ENST00000647720.2:c.3420G>T
|
ENSP00000497673.2:p.Met1140Ile
|
|
|
ENST00000647978.2:c.*3134G>T
|
ENSP00000497658.1:n.*3134G>T
|
|
|
ENST00000649781.2:c.3237G>T
|
ENSP00000497203.1:p.Met1079Ile
|
|
|
ENST00000685018.2:c.3420G>T
|
ENSP00000510194.2:p.Met1140Ile
|
|
|
ENST00000687278.2:c.3420G>T
|
ENSP00000509593.2:p.Met1140Ile
|
|
|
ENST00000699585.1:c.3420G>T
|
ENSP00000514456.1:p.Met1140Ile
|
|
|
ENST00000699598.1:c.3420G>T
|
ENSP00000514467.1:p.Met1140Ile
|
|
|
ENST00000699599.1:c.3420G>T
|
ENSP00000514468.1:p.Met1140Ile
|
|
|
ENST00000699600.1:c.3420G>T
|
ENSP00000514469.1:p.Met1140Ile
|
|
|
ENST00000699601.1:c.*1795G>T
|
ENSP00000514470.1:n.*1795G>T
|
|
|
ENST00000699602.1:c.3414G>T
|
ENSP00000514471.1:p.Met1138Ile
|
|
|
ENST00000699604.1:c.*3244G>T
|
ENSP00000514472.1:n.*3244G>T
|
|
|
ENST00000699605.1:c.2994G>T
|
ENSP00000514473.1:p.Met998Ile
|
|
|
ENST00000685018.1:c.168G>T
|
ENSP00000510194.1:p.Met56Ile
|
|
|
ENST00000687278.1:c.1011G>T
|
ENSP00000509593.1:p.Met337Ile
|
|
|
ENST00000689011.1:c.2G>T
|
|
|
|
ENST00000003084.11:c.3420G>T
MANE Select
|
ENSP00000003084.6:p.Met1140Ile
|
|
|
ENST00000647720.1:c.1070G>T
|
|
|
|
ENST00000648260.1:c.2202G>T
|
ENSP00000497957.1:p.Met734Ile
|
|
|
ENST00000649406.1:c.3237G>T
|
ENSP00000497965.1:p.Met1079Ile
|
|
|
ENST00000649781.1:c.3237G>T
|
ENSP00000497203.1:p.Met1079Ile
|
|
|
ENST00000003084.10:c.3420G>T
|
ENSP00000003084.6:p.Met1140Ile
|
|
|
ENST00000426809.5:c.3330G>T
|
ENSP00000389119.1:p.Met1110Ile
|
|
|
ENST00000468795.1:c.245G>T
|
|
|
|
NM_000492.3:c.3420G>T , LRG_663t1:c.3420G>T
|
NP_000483.3:p.Met1140Ile
|
|
|
XM_011515751.1:c.3510G>T
|
XP_011514053.1:p.Met1170Ile
|
|
|
XM_011515752.1:c.3510G>T
|
XP_011514054.1:p.Met1170Ile
|
|
|
XM_011515753.1:c.3177G>T
|
XP_011514055.1:p.Met1059Ile
|
|
|
XM_011515754.1:c.3177G>T
|
XP_011514056.1:p.Met1059Ile
|
|
|
NM_000492.4:c.3420G>T
MANE Select
|
NP_000483.3:p.Met1140Ile
|
|
