ENST00000211998.10:c.2834T=
MANE Select
|
ENSP00000211998.5:p.Met945=
|
|
ENST00000211998.8:c.2834T=
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ENSP00000211998.4:p.Met945=
|
|
ENST00000372755.7:c.2746-2187T=
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ENSP00000361841.3:n.2746-2187T=
|
|
ENST00000436396.1:c.1850T=
|
ENSP00000415489.1:p.Met617=
|
|
ENST00000623461.3:n.5549-2187T=
|
|
|
ENST00000624354.3:c.*2589T=
|
ENSP00000485551.1:n.*2589T=
|
|
NM_003373.3:c.2746-2187T=
|
NP_003364.1:n.2746-2187T=
|
|
NM_014000.2:c.2834T= , LRG_383t1:c.2834T=
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NP_054706.1:p.Met945=
|
|
XM_005270142.1:c.2837T=
|
XP_005270199.1:p.Met946=
|
|
XM_005270143.1:c.2749-2187T=
|
XP_005270200.1:n.2749-2187T=
|
|
NM_003373.4:c.2746-2187T=
|
NP_003364.1:n.2746-2187T=
|
|
NM_014000.3:c.2834T=
MANE Select
|
NP_054706.1:p.Met945=
|
|