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ENST00000333646.11:c.4100T=
|
ENSP00000333125.8:p.Met1367=
|
|
|
ENST00000374102.6:c.4220T=
|
ENSP00000363215.2:p.Met1407=
|
|
|
ENST00000685182.1:n.853T=
|
|
|
|
ENST00000685655.1:c.173T=
|
ENSP00000509298.1:p.Met58=
|
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|
ENST00000686169.1:n.597T=
|
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|
|
ENST00000686548.1:c.*4116T=
|
ENSP00000509582.1:n.*4116T=
|
|
|
ENST00000687161.1:n.935T=
|
|
|
|
ENST00000687382.1:c.4220T=
|
ENSP00000510724.1:p.Met1407=
|
|
|
ENST00000687701.1:n.849T=
|
|
|
|
ENST00000688079.1:n.2215T=
|
|
|
|
ENST00000688663.1:c.*1141T=
|
ENSP00000509348.1:n.*1141T=
|
|
|
ENST00000688881.1:n.874T=
|
|
|
|
ENST00000688993.1:n.421T=
|
|
|
|
ENST00000689768.1:n.2830T=
|
|
|
|
ENST00000690145.1:c.4220T=
|
ENSP00000508818.1:p.Met1407=
|
|
|
ENST00000690242.1:c.4220T=
|
ENSP00000510090.1:p.Met1407=
|
|
|
ENST00000690250.1:n.1889T=
|
|
|
|
ENST00000690690.1:c.673T=
|
|
|
|
ENST00000690828.1:n.4476T=
|
|
|
|
ENST00000691113.1:c.2699T=
|
ENSP00000509755.1:n.2699T=
|
|
|
ENST00000691426.1:n.3349T=
|
|
|
|
ENST00000691468.1:c.4169T=
|
ENSP00000509011.1:p.Met1390=
|
|
|
ENST00000691909.1:n.940T=
|
|
|
|
ENST00000692304.1:c.4220T=
|
ENSP00000508427.1:p.Met1407=
|
|
|
ENST00000692893.1:n.1529T=
|
|
|
|
ENST00000692964.1:n.884T=
|
|
|
|
ENST00000693050.1:n.727T=
|
|
|
|
ENST00000693324.1:c.4184T=
|
ENSP00000508643.1:p.Met1395=
|
|
|
ENST00000693391.1:c.2165T=
|
ENSP00000509563.1:p.Met722=
|
|
|
ENST00000374080.8:c.4220T=
MANE Select
|
ENSP00000363193.3:p.Met1407=
|
|
|
ENST00000333646.10:c.3761T=
|
ENSP00000333125.7:p.Met1254=
|
|
|
ENST00000374080.7:c.4220T=
|
ENSP00000363193.3:p.Met1407=
|
|
|
ENST00000374102.5:c.4220T=
|
ENSP00000363215.1:p.Met1407=
|
|
|
NM_005120.2:c.4220T=
|
NP_005111.2:p.Met1407=
|
|
|
XM_005262317.1:c.4220T=
|
XP_005262374.1:p.Met1407=
|
|
|
XM_005262319.1:c.4220T=
|
XP_005262376.1:p.Met1407=
|
|
|
NM_005120.3:c.4220T=
MANE Select
|
NP_005111.2:p.Met1407=
|
|
