ENST00000372470.9:c.269G=
MANE Select
|
ENSP00000361548.3:p.Arg90=
|
|
ENST00000413998.7:c.248G=
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ENSP00000414004.3:p.Arg83=
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|
ENST00000638732.1:n.269G=
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|
|
ENST00000372470.7:c.269G=
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ENSP00000361548.3:p.Arg90=
|
|
ENST00000413998.6:c.269G=
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ENSP00000414004.2:p.Arg90=
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|
ENST00000612993.1:c.269G=
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ENSP00000480273.1:p.Arg90=
|
|
NM_005373.2:c.269G= , LRG_510t1:c.269G=
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NP_005364.1:p.Arg90=
|
|
XM_011541478.1:c.248G=
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XP_011539780.1:p.Arg83=
|
|
XM_017001320.1:c.440G=
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XP_016856809.1:p.Arg147=
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|
NM_005373.3:c.269G=
MANE Select
|
NP_005364.1:p.Arg90=
|
|