ENST00000367574.9:c.236G>T
|
ENSP00000356546.6:p.Ser79Ile
|
|
ENST00000537758.6:c.236G>T
|
ENSP00000446401.3:p.Ser79Ile
|
|
ENST00000682661.1:n.395G>T
|
|
|
ENST00000683923.1:c.236G>T
|
ENSP00000506737.1:p.Ser79Ile
|
|
ENST00000684722.1:n.418G>T
|
|
|
ENST00000326194.11:c.236G>T
MANE Select
|
ENSP00000322304.6:p.Ser79Ile
|
|
ENST00000485288.7:c.165G>T
|
ENSP00000420445.3:p.Gln55His
|
|
ENST00000326194.10:c.236G>T
|
ENSP00000322304.6:p.Ser79Ile
|
|
ENST00000355092.4:c.101G>T
|
ENSP00000347207.4:p.Ser34Ile
|
|
ENST00000355961.8:c.236G>T
|
ENSP00000348233.4:p.Ser79Ile
|
|
ENST00000359882.8:c.236G>T
|
ENSP00000352946.4:p.Ser79Ile
|
|
ENST00000361988.7:c.236G>T
|
ENSP00000354978.3:p.Ser79Ile
|
|
ENST00000367574.8:c.236G>T
|
ENSP00000356546.5:p.Ser79Ile
|
|
ENST00000470275.2:c.165G>T
|
ENSP00000418644.2:p.Gln55His
|
|
ENST00000472520.5:c.137-498G>T
|
ENSP00000419858.1:n.137-498G>T
|
|
ENST00000485288.6:c.357G>T
|
ENSP00000420445.2:p.Gln119His
|
|
ENST00000489940.5:c.236G>T
|
ENSP00000419212.1:p.Ser79Ile
|
|
ENST00000491243.5:n.275G>T
|
|
|
ENST00000528612.5:c.165G>T
|
ENSP00000431224.1:p.Gln55His
|
|
ENST00000537758.5:c.236G>T
|
ENSP00000446401.2:p.Ser79Ile
|
|
NM_001282167.1:c.23G>T
|
NP_001269096.1:p.Ser8Ile
|
|
NM_022825.3:c.236G>T
|
NP_073736.2:p.Ser79Ile
|
|
NM_203473.2:c.236G>T
|
NP_982299.1:p.Ser79Ile
|
|
NM_203474.1:c.236G>T
|
NP_982300.1:p.Ser79Ile
|
|
NM_203475.2:c.236G>T
|
NP_982301.1:p.Ser79Ile
|
|
XM_005272635.1:c.575G>T
|
XP_005272692.1:p.Ser192Ile
|
|
XM_005272636.1:c.575G>T
|
XP_005272693.1:p.Ser192Ile
|
|
XM_005272637.1:c.488G>T
|
XP_005272694.1:p.Ser163Ile
|
|
XM_006724544.2:c.341G>T
|
XP_006724607.1:p.Ser114Ile
|
|
XM_006724545.2:c.287G>T
|
XP_006724608.1:p.Ser96Ile
|
|
XM_006724546.2:c.236G>T
|
XP_006724609.1:p.Ser79Ile
|
|
XM_006724547.1:c.23G>T
|
XP_006724610.1:p.Ser8Ile
|
|
XM_011543948.1:c.23G>T
|
XP_011542250.1:p.Ser8Ile
|
|
XM_024452425.1:c.575G>T
|
XP_024308193.1:p.Ser192Ile
|
|
NM_001282167.2:c.23G>T
|
NP_001269096.1:p.Ser8Ile
|
|
NM_022825.4:c.236G>T
|
NP_073736.2:p.Ser79Ile
|
|
NM_203473.3:c.236G>T
|
NP_982299.1:p.Ser79Ile
|
|
NM_203475.3:c.236G>T
MANE Select
|
NP_982301.1:p.Ser79Ile
|
|