ENST00000367400.8:c.4195C=
MANE Select
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ENSP00000356370.3:p.Pro1399=
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ENST00000367399.6:c.3859C=
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ENSP00000356369.2:p.Pro1287=
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ENST00000367400.7:c.4195C=
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ENSP00000356370.3:p.Pro1399=
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ENST00000448952.1:c.429C=
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ENSP00000395407.1:n.429C=
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ENST00000484075.5:c.*306C=
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ENSP00000433932.1:n.*306C=
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ENST00000535699.5:c.4123C=
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ENSP00000438786.1:p.Pro1375=
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ENST00000538660.5:c.2587C=
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ENSP00000438091.1:p.Pro863=
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NM_001193640.1:c.3859C=
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NP_001180569.1:p.Pro1287=
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NM_001257965.1:c.4123C=
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NP_001244894.1:p.Pro1375=
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NM_001257966.1:c.2587C=
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NP_001244895.1:p.Pro863=
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NM_201253.2:c.4195C=
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NP_957705.1:p.Pro1399=
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NR_047563.1:n.4196C=
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NR_047564.1:n.4646C=
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XM_011509366.1:c.*300C=
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XP_011507668.1:n.*300C=
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XM_011509367.1:c.*174C=
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XP_011507669.1:n.*174C=
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XM_011509368.1:c.3613C=
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XP_011507670.1:p.Pro1205=
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XM_011509369.1:c.2638C=
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XP_011507671.1:p.Pro880=
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XM_011509369.2:c.2638C=
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XP_011507671.1:p.Pro880=
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XM_017000851.1:c.3352C=
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XP_016856340.1:p.Pro1118=
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XM_017000852.1:c.4330C=
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XP_016856341.1:p.Pro1444=
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NM_201253.3:c.4195C=
MANE Select
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NP_957705.1:p.Pro1399=
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NM_001193640.2:c.3859C=
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NP_001180569.1:p.Pro1287=
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NM_001257965.2:c.4123C=
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NP_001244894.1:p.Pro1375=
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NR_047563.2:n.4148C=
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NR_047564.2:n.4598C=
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NM_001257966.2:c.2587C=
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NP_001244895.1:p.Pro863=
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