ENST00000330498.4:c.1380T=
MANE Select
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ENSP00000327943.3:p.Ser460=
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ENST00000330498.3:c.1380T=
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ENSP00000327943.3:p.Ser460=
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|
ENST00000419665.6:c.1130-144T=
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ENSP00000410601.2:n.1130-144T=
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ENST00000568188.1:n.751T=
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|
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ENST00000568891.1:n.282-144T=
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NM_003041.3:c.1380T=
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NP_003032.1:p.Ser460=
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|
NR_130783.1:n.1149-144T=
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|
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XM_006721072.2:c.1401T=
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XP_006721135.2:p.Ser467=
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|
XM_006721073.2:c.1302-144T=
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XP_006721136.2:n.1302-144T=
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XM_006721072.4:c.1401T=
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XP_006721135.2:p.Ser467=
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|
XM_024450402.1:c.1151-144T=
|
XP_024306170.1:n.1151-144T=
|
|
NM_003041.4:c.1380T=
MANE Select
|
NP_003032.1:p.Ser460=
|
|
NR_130783.2:n.1144-144T=
|
|
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