ENST00000262493.12:c.730A>G
MANE Select
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ENSP00000262493.6:p.Met244Val
|
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ENST00000562316.6:c.397A>G
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ENSP00000457238.2:p.Met133Val
|
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ENST00000564727.2:c.34A>G
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ENSP00000454971.2:p.Met12Val
|
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ENST00000568375.2:c.116-3476A>G
|
|
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ENST00000638185.1:n.945A>G
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|
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ENST00000638210.1:n.1030A>G
|
|
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ENST00000638705.1:c.730A>G
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ENSP00000491223.1:p.Met244Val
|
|
ENST00000638836.1:n.640A>G
|
|
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ENST00000639055.1:n.1451A>G
|
|
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ENST00000639251.1:n.631A>G
|
|
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ENST00000639268.1:c.365A>G
|
|
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ENST00000639341.1:c.255A>G
|
|
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ENST00000639770.1:c.768A>G
|
ENSP00000491999.1:n.768A>G
|
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ENST00000640390.1:n.660A>G
|
|
|
ENST00000640469.1:c.94A>G
|
ENSP00000491875.1:p.Met32Val
|
|
ENST00000640560.1:n.506A>G
|
|
|
ENST00000640893.1:c.*128A>G
|
ENSP00000492677.1:n.*128A>G
|
|
ENST00000262493.10:c.730A>G
|
ENSP00000262493.6:p.Met244Val
|
|
ENST00000568375.1:n.116-3476A>G
|
|
|
NM_020988.2:c.730A>G
|
NP_066268.1:p.Met244Val
|
|
XM_011523003.1:c.604A>G
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XP_011521305.1:p.Met202Val
|
|
XM_011523003.3:c.604A>G
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XP_011521305.1:p.Met202Val
|
|
NM_020988.3:c.730A>G
MANE Select
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NP_066268.1:p.Met244Val
|
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