ENST00000281928.9:c.3079G>T
MANE Select
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ENSP00000281928.3:p.Ala1027Ser
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ENST00000548743.2:c.3049G>T
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ENSP00000448553.2:p.Ala1017Ser
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ENST00000549786.2:c.2507G>T
|
|
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ENST00000648173.1:n.1874G>T
|
|
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ENST00000648379.1:n.1447G>T
|
|
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ENST00000648737.1:n.2843G>T
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|
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ENST00000648916.1:n.1090G>T
|
|
|
ENST00000649607.1:c.1263G>T
|
|
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ENST00000650226.1:c.3079G>T
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ENSP00000496981.1:p.Ala1027Ser
|
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ENST00000281928.7:c.3079G>T
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ENSP00000281928.3:p.Ala1027Ser
|
|
NM_015335.4:c.3079G>T
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NP_056150.1:p.Ala1027Ser
|
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XM_011538080.1:c.3079G>T
|
XP_011536382.1:p.Ala1027Ser
|
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XM_011538081.1:c.3076G>T
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XP_011536383.1:p.Ala1026Ser
|
|
XM_011538082.1:c.3049G>T
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XP_011536384.1:p.Ala1017Ser
|
|
XM_011538080.2:c.3079G>T
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XP_011536382.1:p.Ala1027Ser
|
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XM_011538081.2:c.3076G>T
|
XP_011536383.1:p.Ala1026Ser
|
|
XM_011538082.2:c.3049G>T
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XP_011536384.1:p.Ala1017Ser
|
|
XM_017019090.1:c.3076G>T
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XP_016874579.1:p.Ala1026Ser
|
|
NM_015335.5:c.3079G>T
MANE Select
|
NP_056150.1:p.Ala1027Ser
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