ENST00000366647.9:c.609G=
MANE Select
|
ENSP00000355607.4:p.Met203=
|
|
ENST00000644483.1:c.*295G=
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ENSP00000496537.1:n.*295G=
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|
ENST00000366647.8:c.609G=
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ENSP00000355607.4:p.Met203=
|
|
ENST00000416000.1:c.579G=
|
ENSP00000411640.1:p.Met193=
|
|
ENST00000436239.5:c.426G=
|
ENSP00000402811.1:p.Met142=
|
|
NM_001316350.1:c.426G=
|
NP_001303279.1:p.Met142=
|
|
NM_014236.3:c.609G=
|
NP_055051.1:p.Met203=
|
|
XM_005273313.3:c.606G=
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XP_005273370.1:p.Met202=
|
|
XM_011544303.1:c.282G=
|
XP_011542605.1:p.Met94=
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|
XM_011544304.1:c.282G=
|
XP_011542606.1:p.Met94=
|
|
XM_005273313.4:c.606G=
|
XP_005273370.1:p.Met202=
|
|
XM_011544303.3:c.282G=
|
XP_011542605.1:p.Met94=
|
|
XM_011544304.2:c.282G=
|
XP_011542606.1:p.Met94=
|
|
NM_014236.4:c.609G=
MANE Select
|
NP_055051.1:p.Met203=
|
|
NM_001316350.2:c.426G=
|
NP_001303279.1:p.Met142=
|
|