ENST00000529510.6:n.1077G>T
|
|
|
ENST00000697845.1:n.1857G>T
|
|
|
ENST00000697846.1:n.1077G>T
|
|
|
ENST00000697847.1:n.1202-261G>T
|
|
|
ENST00000697848.1:n.1163G>T
|
|
|
ENST00000697849.1:n.2972G>T
|
|
|
ENST00000697850.1:n.1163G>T
|
|
|
ENST00000697851.1:n.2771G>T
|
|
|
ENST00000638186.1:n.1237G>T
|
|
|
ENST00000638360.1:n.1069G>T
|
|
|
ENST00000638925.1:n.1202G>T
|
|
|
ENST00000650539.1:n.1339G>T
|
|
|
ENST00000330775.9:c.933G>T
|
ENSP00000476242.2:p.Met311Ile
|
|
ENST00000357590.9:c.933G>T
|
ENSP00000476176.2:p.Met311Ile
|
|
ENST00000524428.5:n.1169G>T
|
|
|
ENST00000525039.5:n.1357G>T
|
|
|
ENST00000525102.5:n.1691G>T
|
|
|
ENST00000525372.5:n.1031G>T
|
|
|
ENST00000526275.5:n.1715G>T
|
|
|
ENST00000527992.5:n.1161G>T
|
|
|
ENST00000529510.5:n.621G>T
|
|
|
ENST00000530407.5:n.1083G>T
|
|
|
ENST00000532085.1:n.4314G>T
|
|
|
ENST00000538950.5:c.714G>T
|
ENSP00000475991.2:p.Met238Ile
|
|
ENST00000545985.5:c.933G>T
|
ENSP00000475241.2:p.Met311Ile
|
|
NM_001164277.1:c.933G>T , LRG_187t1:c.933G>T
|
NP_001157749.1:p.Met311Ile
|
|
NM_001164278.1:c.933G>T
|
NP_001157750.1:p.Met311Ile
|
|
NM_001164279.1:c.714G>T
|
NP_001157751.1:p.Met238Ile
|
|
NM_001164280.1:c.933G>T
|
NP_001157752.1:p.Met311Ile
|
|
NM_001467.5:c.933G>T
|
NP_001458.1:p.Met311Ile
|
|
NM_001164278.2:c.933G>T
|
NP_001157750.1:p.Met311Ile
|
|
NM_001164279.2:c.714G>T
|
NP_001157751.1:p.Met238Ile
|
|
NM_001164280.2:c.933G>T
|
NP_001157752.1:p.Met311Ile
|
|
NM_001467.6:c.933G>T
|
NP_001458.1:p.Met311Ile
|
|
NM_001164277.2:c.933G>T
MANE Select
|
NP_001157749.1:p.Met311Ile
|
|