ENST00000217260.9:c.194A=
MANE Select
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ENSP00000217260.4:p.Gln65=
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|
ENST00000217260.8:c.194A=
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ENSP00000217260.4:p.Gln65=
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|
ENST00000400634.2:c.194A=
|
ENSP00000383475.2:p.Gln65=
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|
NM_001029871.3:c.194A=
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NP_001025042.2:p.Gln65=
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|
NM_001040007.2:c.194A=
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NP_001035096.1:p.Gln65=
|
|
XM_011529232.1:c.242A=
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XP_011527534.1:p.Gln81=
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|
XM_011529233.1:c.242A=
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XP_011527535.1:p.Gln81=
|
|
XR_937068.1:n.314A=
|
|
|
XR_937069.1:n.309A=
|
|
|
XM_017027839.1:c.194A=
|
XP_016883328.1:p.Gln65=
|
|
NM_001029871.4:c.194A=
MANE Select
|
NP_001025042.2:p.Gln65=
|
|
NM_001040007.3:c.194A=
|
NP_001035096.1:p.Gln65=
|
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