ENST00000367698.4:c.1342C>G
MANE Select
|
ENSP00000356671.3:p.Pro448Ala
|
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ENST00000367698.3:c.1342C>G
|
ENSP00000356671.3:p.Pro448Ala
|
|
ENST00000617423.4:c.727C>G
|
ENSP00000478688.1:p.Pro243Ala
|
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NM_000488.3:c.1342C>G , LRG_577t1:c.1342C>G
|
NP_000479.1:p.Pro448Ala
|
|
XM_005245198.2:c.1198C>G
|
XP_005245255.1:p.Pro400Ala
|
|
NM_001365052.1:c.1198C>G
|
NP_001351981.1:p.Pro400Ala
|
|
NM_000488.4:c.1342C>G
MANE Select
|
NP_000479.1:p.Pro448Ala
|
|
NM_001365052.2:c.1198C>G
|
NP_001351981.1:p.Pro400Ala
|
|
NM_001386302.1:c.1465C>G
|
NP_001373231.1:p.Pro489Ala
|
|
NM_001386303.1:c.1423C>G
|
NP_001373232.1:p.Pro475Ala
|
|
NM_001386304.1:c.1321C>G
|
NP_001373233.1:p.Pro441Ala
|
|
NM_001386305.1:c.1285C>G
|
NP_001373234.1:p.Pro429Ala
|
|
NM_001386306.1:c.1126C>G
|
NP_001373235.1:p.Pro376Ala
|
|