ENST00000651671.1:c.6494G>C
MANE Select
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ENSP00000498587.1:p.Gly2165Ala
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ENST00000679595.1:c.*1534G>C
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ENSP00000506241.1:n.*1534G>C
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ENST00000679969.1:n.3090G>C
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ENST00000680003.1:n.2826G>C
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ENST00000680133.1:c.6380G>C
|
ENSP00000505319.1:p.Gly2127Ala
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ENST00000680218.1:c.6374G>C
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ENSP00000505339.1:p.Gly2125Ala
|
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ENST00000680668.1:c.6380G>C
|
ENSP00000506336.1:p.Gly2127Ala
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ENST00000680778.1:c.4091G>C
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ENSP00000506033.1:p.Gly1364Ala
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ENST00000680924.1:c.*3894G>C
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ENSP00000506031.1:n.*3894G>C
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ENST00000681135.1:c.*4103G>C
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ENSP00000506636.1:n.*4103G>C
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ENST00000681298.1:n.4599G>C
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ENST00000681454.1:c.*5730G>C
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ENSP00000505763.1:n.*5730G>C
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ENST00000277541.6:c.6494G>C
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ENSP00000277541.6:p.Gly2165Ala
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NM_017617.3:c.6494G>C
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NP_060087.3:p.Gly2165Ala
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XM_011518717.1:c.5795G>C
|
XP_011517019.1:p.Gly1932Ala
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NM_017617.5:c.6494G>C
MANE Select
|
NP_060087.3:p.Gly2165Ala
|
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XM_011518717.2:c.5771G>C
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XP_011517019.2:p.Gly1924Ala
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