|
ENST00000323851.13:c.714G>C
MANE Select
|
ENSP00000319977.8:p.Glu238Asp
|
|
|
ENST00000537882.3:c.714G>C
|
ENSP00000437443.2:p.Glu238Asp
|
|
|
ENST00000675056.1:n.44G>C
|
|
|
|
ENST00000675068.1:c.16G>C
|
|
|
|
ENST00000675172.1:c.310G>C
|
ENSP00000502297.1:n.310G>C
|
|
|
ENST00000675273.1:n.73G>C
|
|
|
|
ENST00000675860.1:n.479G>C
|
|
|
|
ENST00000676444.1:n.745G>C
|
|
|
|
ENST00000323851.11:c.714G>C
|
ENSP00000319977.7:p.Glu238Asp
|
|
|
ENST00000414097.6:c.714G>C
|
ENSP00000404854.2:p.Glu238Asp
|
|
|
ENST00000517331.5:n.432G>C
|
|
|
|
ENST00000517599.5:c.*320G>C
|
ENSP00000429172.1:n.*320G>C
|
|
|
ENST00000518066.5:c.37-6700G>C
|
ENSP00000431057.1:n.37-6700G>C
|
|
|
ENST00000518176.5:c.49-2093G>C
|
ENSP00000429007.1:n.49-2093G>C
|
|
|
ENST00000519278.5:n.1810G>C
|
|
|
|
ENST00000521414.5:n.176G>C
|
|
|
|
ENST00000521664.1:n.464G>C
|
|
|
|
ENST00000522377.5:c.*194G>C
|
ENSP00000429380.1:n.*194G>C
|
|
|
ENST00000522476.5:c.516G>C
|
ENSP00000427894.1:p.Glu172Asp
|
|
|
ENST00000522665.5:n.37G>C
|
|
|
|
ENST00000537882.2:c.471G>C
|
ENSP00000437443.1:p.Glu157Asp
|
|
|
NM_001135242.1:c.714G>C
|
NP_001128714.1:p.Glu238Asp
|
|
|
NM_001258432.1:c.516G>C
|
NP_001245361.1:p.Glu172Asp
|
|
|
NM_001258433.1:c.471G>C
|
NP_001245362.1:p.Glu157Asp
|
|
|
NM_006096.3:c.714G>C , LRG_258t1:c.714G>C
|
NP_006087.2:p.Glu238Asp
|
|
|
XM_011516791.1:c.765G>C
|
XP_011515093.1:p.Glu255Asp
|
|
|
XM_011516792.1:c.147G>C
|
XP_011515094.1:p.Glu49Asp
|
|
|
XM_011516792.2:c.147G>C
|
XP_011515094.1:p.Glu49Asp
|
|
|
NM_001135242.2:c.714G>C
|
NP_001128714.1:p.Glu238Asp
|
|
|
NM_001258432.2:c.516G>C
|
NP_001245361.1:p.Glu172Asp
|
|
|
NM_001258433.2:c.471G>C
|
NP_001245362.1:p.Glu157Asp
|
|
|
NM_001374844.1:c.765G>C
|
NP_001361773.1:p.Glu255Asp
|
|
|
NM_001374845.1:c.714G>C
|
NP_001361774.1:p.Glu238Asp
|
|
|
NM_001374846.1:c.714G>C
|
NP_001361775.1:p.Glu238Asp
|
|
|
NM_001374847.1:c.516G>C
|
NP_001361776.1:p.Glu172Asp
|
|
|
NM_006096.4:c.714G>C
MANE Select
|
NP_006087.2:p.Glu238Asp
|
|
