ENST00000360256.9:c.6455_6456delinsCT
MANE Select
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ENSP00000353393.4:p.Ser2152=
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|
ENST00000644698.1:c.188_189delinsCT
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ENSP00000495706.1:p.Ser63=
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|
ENST00000330287.10:c.50_51delinsCT
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ENSP00000327895.6:p.Ser17=
|
|
ENST00000360256.8:c.6455_6456delinsCT
|
ENSP00000353393.4:p.Ser2152=
|
|
NM_000132.3:c.6455_6456delinsCT
|
NP_000123.1:p.Ser2152=
|
|
NM_019863.2:c.50_51delinsCT
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NP_063916.1:p.Ser17=
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|
XM_011531126.1:c.6350_6351delinsCT
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XP_011529428.1:p.Ser2117=
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|
NM_000132.4:c.6455_6456delinsCT
MANE Select
|
NP_000123.1:p.Ser2152=
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|
NM_019863.3:c.50_51delinsCT
|
NP_063916.1:p.Ser17=
|
|