ENST00000372470.9:c.1514G=
MANE Select
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ENSP00000361548.3:p.Ser505=
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|
ENST00000413998.7:c.1493G=
|
ENSP00000414004.3:p.Ser498=
|
|
ENST00000638732.1:n.1514G=
|
|
|
ENST00000643351.1:c.46G=
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|
|
ENST00000372470.7:c.1514G=
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ENSP00000361548.3:p.Ser505=
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|
ENST00000413998.6:c.1514G=
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ENSP00000414004.2:p.Ser505=
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|
ENST00000612993.1:c.1514G=
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ENSP00000480273.1:p.Ser505=
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|
NM_005373.2:c.1514G= , LRG_510t1:c.1514G=
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NP_005364.1:p.Ser505=
|
|
XM_011541478.1:c.1493G=
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XP_011539780.1:p.Ser498=
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|
XM_017001320.1:c.1685G=
|
XP_016856809.1:p.Ser562=
|
|
NM_005373.3:c.1514G=
MANE Select
|
NP_005364.1:p.Ser505=
|
|