ENST00000357060.8:c.3412A>C
MANE Select
|
ENSP00000349568.3:p.Met1138Leu
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ENST00000357060.7:c.3412A>C
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ENSP00000349568.3:p.Met1138Leu
|
|
ENST00000434629.5:c.1494A>C
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|
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NM_025145.5:c.3412A>C
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NP_079421.5:p.Met1138Leu
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|
XM_005270171.1:c.3415A>C
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XP_005270228.1:p.Met1139Leu
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|
XM_005270172.2:c.3415A>C
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XP_005270229.1:p.Met1139Leu
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XM_011540196.1:c.3529A>C
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XP_011538498.1:p.Met1177Leu
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XM_011540197.1:c.3529A>C
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XP_011538499.1:p.Met1177Leu
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|
XM_011540198.1:c.3412A>C
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XP_011538500.1:p.Met1138Leu
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|
XM_011540199.1:c.3412A>C
|
XP_011538501.1:p.Met1138Leu
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|
XM_011540200.1:c.3529A>C
|
XP_011538502.1:p.Met1177Leu
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|
XM_011540201.1:c.3529A>C
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XP_011538503.1:p.Met1177Leu
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|
XM_011540202.1:c.2758A>C
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XP_011538504.1:p.Met920Leu
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|
XM_011540203.1:c.1312A>C
|
XP_011538505.1:p.Met438Leu
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|
NM_025145.6:c.3412A>C
|
NP_079421.5:p.Met1138Leu
|
|
XM_005270171.2:c.3415A>C
|
XP_005270228.1:p.Met1139Leu
|
|
XM_005270172.3:c.3415A>C
|
XP_005270229.1:p.Met1139Leu
|
|
XM_011540196.2:c.3529A>C
|
XP_011538498.1:p.Met1177Leu
|
|
XM_011540197.2:c.3529A>C
|
XP_011538499.1:p.Met1177Leu
|
|
XM_011540198.2:c.3412A>C
|
XP_011538500.1:p.Met1138Leu
|
|
XM_011540199.2:c.3412A>C
|
XP_011538501.1:p.Met1138Leu
|
|
XM_011540200.2:c.3529A>C
|
XP_011538502.1:p.Met1177Leu
|
|
XM_011540201.2:c.3529A>C
|
XP_011538503.1:p.Met1177Leu
|
|
XM_011540202.2:c.2758A>C
|
XP_011538504.1:p.Met920Leu
|
|
XM_017016681.1:c.3526A>C
|
XP_016872170.1:p.Met1176Leu
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|
XM_017016682.1:c.3181A>C
|
XP_016872171.1:p.Met1061Leu
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XM_024448177.1:c.1915A>C
|
XP_024303945.1:p.Met639Leu
|
|
XM_024448178.1:c.1312A>C
|
XP_024303946.1:p.Met438Leu
|
|
XR_002957015.1:n.3298A>C
|
|
|
NM_025145.7:c.3412A>C
MANE Select
|
NP_079421.5:p.Met1138Leu
|
|