ENST00000368845.6:c.1191T>G
MANE Select
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ENSP00000357838.5:p.Leu397=
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ENST00000368845.5:c.1191T>G
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ENSP00000357838.5:p.Leu397=
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ENST00000471127.1:n.701T>G
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|
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ENST00000539214.5:c.777T>G
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ENSP00000439042.1:p.Leu259=
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NM_000274.3:c.1191T>G , LRG_685t1:c.1191T>G
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NP_000265.1:p.Leu397=
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NM_001171814.1:c.777T>G
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NP_001165285.1:p.Leu259=
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XM_006717871.2:c.1191T>G
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XP_006717934.1:p.Leu397=
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XM_011539833.1:c.1191T>G
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XP_011538135.1:p.Leu397=
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XM_011539834.1:c.1191T>G
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XP_011538136.1:p.Leu397=
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NM_001322965.1:c.1191T>G
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NP_001309894.1:p.Leu397=
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NM_001322966.1:c.1191T>G
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NP_001309895.1:p.Leu397=
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NM_001322967.1:c.1191T>G
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NP_001309896.1:p.Leu397=
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NM_001322968.1:c.1191T>G
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NP_001309897.1:p.Leu397=
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NM_001322969.1:c.1191T>G
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NP_001309898.1:p.Leu397=
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NM_001322970.1:c.1191T>G
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NP_001309899.1:p.Leu397=
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NM_001322971.1:c.870T>G
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NP_001309900.1:p.Leu290=
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NM_001322974.1:c.591T>G
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NP_001309903.1:p.Leu197=
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XM_017016279.1:c.591T>G
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XP_016871768.1:p.Leu197=
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NM_000274.4:c.1191T>G
MANE Select
|
NP_000265.1:p.Leu397=
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|
NM_001322965.2:c.1191T>G
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NP_001309894.1:p.Leu397=
|
|
NM_001322966.2:c.1191T>G
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NP_001309895.1:p.Leu397=
|
|
NM_001322967.2:c.1191T>G
|
NP_001309896.1:p.Leu397=
|
|
NM_001322968.2:c.1191T>G
|
NP_001309897.1:p.Leu397=
|
|
NM_001322969.2:c.1191T>G
|
NP_001309898.1:p.Leu397=
|
|
NM_001322970.2:c.1191T>G
|
NP_001309899.1:p.Leu397=
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|
NM_001322971.2:c.870T>G
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NP_001309900.1:p.Leu290=
|
|
NM_001322974.2:c.591T>G
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NP_001309903.1:p.Leu197=
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NM_001171814.2:c.777T>G
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NP_001165285.1:p.Leu259=
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