ENST00000528992.2:c.183G=
|
ENSP00000436479.2:p.Met61=
|
|
ENST00000682350.1:c.150G=
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ENSP00000508090.1:p.Met50=
|
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ENST00000682764.1:c.150G=
|
ENSP00000506780.1:p.Met50=
|
|
ENST00000339994.5:c.411G=
MANE Select
|
ENSP00000345708.4:p.Met137=
|
|
ENST00000339994.4:c.411G=
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ENSP00000345708.4:p.Met137=
|
|
ENST00000526912.1:c.150G=
|
ENSP00000432729.1:p.Met50=
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ENST00000528731.1:c.150G=
|
ENSP00000434755.1:p.Met50=
|
|
ENST00000528992.1:c.428G=
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|
|
NM_000525.3:c.411G=
|
NP_000516.3:p.Met137=
|
|
NM_001166290.1:c.150G=
|
NP_001159762.1:p.Met50=
|
|
XM_006718226.2:c.150G=
|
XP_006718289.1:p.Met50=
|
|
XR_930867.1:n.569G=
|
|
|
XM_006718226.3:c.150G=
|
XP_006718289.1:p.Met50=
|
|
XM_017017680.1:c.150G=
|
XP_016873169.1:p.Met50=
|
|
NM_001166290.2:c.150G=
|
NP_001159762.1:p.Met50=
|
|
NM_001377296.1:c.150G=
|
NP_001364225.1:p.Met50=
|
|
NM_001377297.1:c.150G=
|
NP_001364226.1:p.Met50=
|
|
NM_000525.4:c.411G=
MANE Select
|
NP_000516.3:p.Met137=
|
|