ENST00000333371.8:c.2T=
MANE Select
|
ENSP00000327650.4:p.Met1=
|
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ENST00000643536.1:c.2T=
|
ENSP00000494429.1:p.Met1=
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|
ENST00000647331.1:c.2T=
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ENSP00000493953.1:p.Met1=
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ENST00000333371.7:c.2T=
|
ENSP00000327650.3:p.Met1=
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|
ENST00000535906.1:c.2T=
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ENSP00000444053.1:p.Met1=
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|
ENST00000556096.6:n.356T=
|
|
|
ENST00000557358.1:n.349T=
|
|
|
ENST00000574755.5:c.2T=
|
ENSP00000460413.1:p.Met1=
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|
NM_001289148.1:c.2T=
|
NP_001276077.1:p.Met1=
|
|
NM_001289149.1:c.-210T=
|
NP_001276078.1:n.-210T=
|
|
NM_018668.4:c.2T= , LRG_884t1:c.2T=
|
NP_061138.3:p.Met1=
|
|
XM_005254884.2:c.2T=
|
XP_005254941.1:p.Met1=
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|
XM_005254887.1:c.-129T=
|
XP_005254944.1:n.-129T=
|
|
XM_005254888.2:c.2T=
|
XP_005254945.1:p.Met1=
|
|
XM_011521448.1:c.-312T=
|
XP_011519750.1:n.-312T=
|
|
XM_017022075.2:c.-360T=
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XP_016877564.1:n.-360T=
|
|
XM_017022076.1:c.-217T=
|
XP_016877565.1:n.-217T=
|
|
XR_001751213.2:n.338T=
|
|
|
NM_018668.5:c.2T=
MANE Select
|
NP_061138.3:p.Met1=
|
|