ENST00000644269.2:c.2124_2125delinsCT
MANE Select
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ENSP00000494017.1:p.Phe708=
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ENST00000644846.1:c.780_781delinsCT
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|
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ENST00000265715.7:c.2124_2125delinsCT
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ENSP00000265715.3:p.Phe708=
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ENST00000492030.2:n.377-67_377-66delinsCT
|
|
|
NM_000441.1:c.2124_2125delinsCT
|
NP_000432.1:p.Phe708=
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XM_005250425.1:c.2124_2125delinsCT
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XP_005250482.1:p.Phe708=
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|
XM_005250425.2:c.2124_2125delinsCT
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XP_005250482.1:p.Phe708=
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XM_017012318.1:c.2046_2047delinsCT
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XP_016867807.1:p.Phe682=
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|
NM_000441.2:c.2124_2125delinsCT
MANE Select
|
NP_000432.1:p.Phe708=
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